geneid | 57467 |
---|---|
ensemblid | ENSG00000010282.15 |
hgncid | 13242 |
symbol | HHATL |
name | hedgehog acyltransferase like |
refseq_nuc | NM_020707.4 |
refseq_prot | NP_065758.3 |
ensembl_nuc | ENST00000441594.6 |
ensembl_prot | ENSP00000405423.1 |
mane_status | MANE Select |
chr | chr3 |
start | 42692663 |
end | 42702798 |
strand | - |
ver | v1.2 |
region | chr3:42692663-42702798 |
region5000 | chr3:42687663-42707798 |
regionname0 | HHATL_chr3_42692663_42702798 |
regionname5000 | HHATL_chr3_42687663_42707798 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 504 | 269 | 60 | 54 | 113 | 10 | 32 | 83 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002 | 1/0 | 504 | 129 | 29 | 27 | 55 | 3 | 14 | 47 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0003 | 0/0 | 504 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0004 | 0/0 | 504 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0005 | 0/0 | 504 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0006 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0007 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0008 | 0/0 | 504 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0009 | 0/1 | 504 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0010 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0011 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0012 | 0/0 | 504 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
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 | 0/0 | 1515 | 246 | 51 | 54 | 100 | 10 | 31 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0002 | 1/0 | 1515 | 83 | 14 | 19 | 32 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0003 | 0/0 | 1515 | 29 | 0 | 6 | 23 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0004 | 0/0 | 1515 | 14 | 14 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0005 | 0/0 | 1515 | 12 | 0 | 0 | 12 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0006 | 0/0 | 1515 | 5 | 4 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0007 | 0/0 | 1515 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0008 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0009 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0010 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0011 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0012 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0013 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0014 | 0/1 | 1515 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0015 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0016 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0017 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0018 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0019 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0020 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0021 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
c0022 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 322 | 411 | 93 | 86 | 170 | 14 | 46 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
t0002 | 0/0 | 322 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 96 | 15 | 18 | 52 | 3 | 8 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0002 | 0/0 | 45 | 2 | 7 | 19 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0003 | 0/0 | 26 | 0 | 6 | 20 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0004 | 1/0 | 19 | 1 | 11 | 0 | 0 | 6 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0005 | 0/0 | 12 | 7 | 2 | 1 | 0 | 2 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0006 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0009 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0010 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0011 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0013 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0017 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
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 | 0/0 | 1515 | 246 | 51 | 54 | 100 | 10 | 31 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0005 | 0/0 | 1515 | 12 | 0 | 0 | 12 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0006 | 0/0 | 1515 | 5 | 4 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0008 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0012 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0019 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0020 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0002 | 1/0 | 1515 | 83 | 14 | 19 | 32 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0003 | 0/0 | 1515 | 29 | 0 | 6 | 23 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0004 | 0/0 | 1515 | 14 | 14 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0011 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0017 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0003c0007 | 0/0 | 1515 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0004c0010 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0005c0009 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0006c0013 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0007c0016 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0008c0015 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0009c0014 | 0/1 | 1515 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0010c0018 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0011c0021 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0012c0022 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1836 | 246 | 51 | 54 | 100 | 10 | 31 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0005t0001 | 0/0 | 1836 | 12 | 0 | 0 | 12 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0006t0001 | 0/0 | 1836 | 5 | 4 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0008t0001 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0012t0001 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0019t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0001c0020t0001 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0002t0001 | 1/0 | 1836 | 83 | 14 | 19 | 32 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0003t0001 | 0/0 | 1836 | 29 | 0 | 6 | 23 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0004t0001 | 0/0 | 1836 | 13 | 13 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0004t0002 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0011t0001 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0002c0017t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0003c0007t0001 | 0/0 | 1836 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0004c0010t0001 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0005c0009t0001 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0006c0013t0001 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0007c0016t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0008c0015t0001 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0009c0014t0001 | 0/1 | 1836 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0010c0018t0001 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0011c0021t0001 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
a0012c0022t0001 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | copy fasta | chr3 | 42687663 | 42707798 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 96 | 15 | 18 | 52 | 3 | 8 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0002 | 0/0 | 45 | 2 | 7 | 19 | 3 | 14 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0013 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0005t0001g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0006t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0008t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0012t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0019t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0001c0020t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0004 | 1/0 | 19 | 1 | 11 | 0 | 0 | 6 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0005 | 0/0 | 12 | 7 | 2 | 1 | 0 | 2 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0009 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0010 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0011 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0003t0001g0003 | 0/0 | 26 | 0 | 6 | 20 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0004t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0004t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0004t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0004t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0011t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0002c0017t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0003c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0003c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0003c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0004c0010t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0005c0009t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0006c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0007c0016t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0008c0015t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0009c0014t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0010c0018t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0011c0021t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
a0012c0022t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00323 | hp1 | a0012 | c0022 | t0001 | g0061 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00544 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00609 | hp1 | a0001 | c0005 | t0001 | g0110 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00609 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00738 | hp1 | a0005 | c0009 | t0001 | g0035 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01070 | hp1 | a0004 | c0010 | t0001 | g0037 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01167 | hp1 | a0002 | c0011 | t0001 | g0033 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01169 | hp1 | a0002 | c0011 | t0001 | g0033 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01175 | hp1 | a0004 | c0010 | t0001 | g0037 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01175 | hp2 | a0005 | c0009 | t0001 | g0035 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01361 | hp2 | a0008 | c0015 | t0001 | g0085 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0088 | EUR | IBS | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01891 | hp1 | a0002 | c0004 | t0001 | g0031 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01891 | hp2 | a0001 | c0006 | t0001 | g0047 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01981 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02056 | hp1 | a0001 | c0005 | t0001 | g0109 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02258 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02273 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02293 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02523 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02615 | hp1 | a0002 | c0004 | t0001 | g0022 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02647 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02647 | hp2 | a0003 | c0007 | t0001 | g0056 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02717 | hp1 | a0002 | c0004 | t0002 | g0117 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02723 | hp2 | a0003 | c0007 | t0001 | g0051 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02809 | hp1 | a0003 | c0007 | t0001 | g0050 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02818 | hp1 | a0001 | c0012 | t0001 | g0032 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02886 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02895 | hp2 | a0001 | c0008 | t0001 | g0029 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02897 | hp2 | a0001 | c0008 | t0001 | g0029 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02922 | hp2 | a0002 | c0004 | t0001 | g0031 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02976 | hp1 | a0001 | c0006 | t0001 | g0027 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03041 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03098 | hp2 | a0002 | c0004 | t0001 | g0022 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03130 | hp2 | a0002 | c0004 | t0001 | g0071 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03209 | hp1 | a0011 | c0021 | t0001 | g0112 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03486 | hp2 | a0002 | c0004 | t0001 | g0022 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03490 | hp1 | a0001 | c0020 | t0001 | g0072 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0012 | AFR | ESN | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18612 | hp2 | a0002 | c0003 | t0001 | g0105 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18906 | hp2 | a0002 | c0017 | t0001 | g0045 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18939 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18940 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18941 | hp1 | a0001 | c0006 | t0001 | g0041 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18950 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18962 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18972 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18973 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18975 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18977 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18979 | hp2 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18980 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18998 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19007 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19009 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19010 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19043 | hp1 | a0001 | c0019 | t0001 | g0078 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19064 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19074 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19084 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19087 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19090 | hp1 | a0010 | c0018 | t0001 | g0055 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19240 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ASW | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | TSI | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02109 | hp2 | a0007 | c0016 | t0001 | g0083 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02486 | hp2 | a0001 | c0012 | t0001 | g0032 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18955 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA18955 | hp2 | a0006 | c0013 | t0001 | g0064 | EAS | JPT | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20300 | hp1 | a0002 | c0004 | t0001 | g0074 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA20300 | hp2 | a0001 | c0006 | t0001 | g0027 | AFR | USA | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
NA21309 | hp2 | a0001 | c0006 | t0001 | g0046 | AFR | LWK | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
homoSapiens_chm13v2 | hp1 | a0009 | c0014 | t0001 | g0067 | REF | REF | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0004 | REF | REF | HHATL_chr3_42687663_42707798 | HHATL | chr3 | 42687663 | 42707798 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42692759
|
G | C | 1 | a0008 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1507C>G | p.Pro503Ala | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 12/12 | 1740/1836 | 1507/1515 | 503/504 | chr3 | 42692759 | ||
chr3:42692803
|
C | T | 1 | a0004 | 2 | HG01070.hp1 HG01175.hp1 |
missense_variant | MODERATE | c.1463G>A | p.Arg488Gln | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 12/12 | 1696/1836 | 1463/1515 | 488/504 | chr3 | 42692803 | ||
chr3:42693095
|
G | C | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1372C>G | p.Arg458Gly | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 11/12 | 1605/1836 | 1372/1515 | 458/504 | chr3 | 42693095 | ||
chr3:42693658
|
T | C | 8 | a0001a0003a0004others(5): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
missense_variant | MODERATE | c.1207A>G | p.Met403Val | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/12 | 1440/1836 | 1207/1515 | 403/504 | chr3 | 42693658 | ||
chr3:42693745
|
C | T | 1 | a0009 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1120G>A | p.Ala374Thr | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/12 | 1353/1836 | 1120/1515 | 374/504 | chr3 | 42693745 | ||
chr3:42697041
|
G | T | 1 | a0005 | 2 | HG00738.hp1 HG01175.hp2 |
missense_variant | MODERATE | c.970C>A | p.Pro324Thr | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/12 | 1203/1836 | 970/1515 | 324/504 | chr3 | 42697041 | ||
chr3:42697547
|
C | A | 1 | a0010 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.826G>T | p.Asp276Tyr | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/12 | 1059/1836 | 826/1515 | 276/504 | chr3 | 42697547 | ||
chr3:42698898
|
C | T | 1 | a0006 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.293G>A | p.Arg98His | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/12 | 526/1836 | 293/1515 | 98/504 | chr3 | 42698898 | ||
chr3:42699061
|
C | A | 1 | a0011 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.259G>T | p.Ala87Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/12 | 492/1836 | 259/1515 | 87/504 | chr3 | 42699061 | ||
chr3:42699084
|
G | A | 1 | a0012 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.236C>T | p.Ala79Val | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/12 | 469/1836 | 236/1515 | 79/504 | chr3 | 42699084 | ||
chr3:42700801
|
G | C | 1 | a0003 | 3 | HG02647.hp2 HG02723.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.26C>G | p.Ala9Gly | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/12 | 259/1836 | 26/1515 | 9/504 | chr3 | 42700801 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42693782
|
A | G | 16 | a0001c0001a0001c0005a0001c0006others(13): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
synonymous_variant | LOW | c.1083T>C | p.Ala361Ala | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/12 | 1316/1836 | 1083/1515 | 361/504 | chr3 | 42693782 | ||
chr3:42697102
|
C | T | 2 | a0001c0008a0002c0003 | 31 | HG01081.hp2 HG01358.hp1 HG01978.hp2 others(28): Show |
synonymous_variant | LOW | c.909G>A | p.Ala303Ala | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/12 | 1142/1836 | 909/1515 | 303/504 | chr3 | 42697102 | ||
chr3:42697536
|
G | A | 2 | a0001c0006a0002c0017 | 6 | HG01891.hp2 HG02976.hp1 NA18906.hp2 others(3): Show |
synonymous_variant | LOW | c.837C>T | p.Phe279Phe | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/12 | 1070/1836 | 837/1515 | 279/504 | chr3 | 42697536 | ||
chr3:42697548
|
G | A | 1 | a0001c0019 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.825C>T | p.Ser275Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/12 | 1058/1836 | 825/1515 | 275/504 | chr3 | 42697548 | ||
chr3:42698244
|
G | A | 1 | a0001c0020 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.591C>T | p.His197His | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/12 | 824/1836 | 591/1515 | 197/504 | chr3 | 42698244 | ||
chr3:42698777
|
G | C | 1 | a0002c0011 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.414C>G | p.Pro138Pro | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/12 | 647/1836 | 414/1515 | 138/504 | chr3 | 42698777 | ||
chr3:42698792
|
C | T | 1 | a0001c0005 | 12 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(9): Show |
synonymous_variant | LOW | c.399G>A | p.Ser133Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/12 | 632/1836 | 399/1515 | 133/504 | chr3 | 42698792 | ||
chr3:42699077
|
G | A | 1 | a0001c0012 | 2 | HG02486.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.243C>T | p.Ser81Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/12 | 476/1836 | 243/1515 | 81/504 | chr3 | 42699077 | ||
chr3:42700767
|
A | G | 1 | a0003c0007 | 3 | HG02647.hp2 HG02723.hp2 HG02809.hp1 |
synonymous_variant | LOW | c.60T>C | p.Ser20Ser | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/12 | 293/1836 | 60/1515 | 20/504 | chr3 | 42700767 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42702591
|
G | A | 1 | a0002c0004t0002 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/12 | 1765 | chr3 | 42702591 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:42692953
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1391-78G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 11/11 | chr3 | 42692953 | ||||||
chr3:42692953
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1391-78G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 11/11 | chr3 | 42692953 | ||||||
chr3:42693258
|
C | A | 11 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0014others(8): Show | 32 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-40G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693258 | ||||||
chr3:42693335
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1249-117C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693335 | ||||||
chr3:42693562
|
G | GC | 17 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0026others(14): Show | 25 | HG01070.hp1 HG01074.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248+54dupG | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693562 | ||||||
chr3:42693568
|
C | A | 1 | a0001c0001t0001g0036 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1248+49G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 10/11 | chr3 | 42693568 | ||||||
chr3:42694131
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1047-313A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694131 | ||||||
chr3:42694159
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1047-341A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694159 | ||||||
chr3:42694349
|
C | G | 1 | a0004c0010t0001g0037 | 2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1047-531G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694349 | ||||||
chr3:42694395
|
A | G | 1 | a0001c0001t0001g0021 | 4 | HG03139.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-577T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694395 | ||||||
chr3:42694470
|
A | G | 3 | a0002c0002t0001g0010a0002c0002t0001g0080a0007c0016t0001g0083 | 9 | HG00099.hp2 HG00733.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1047-652T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694470 | ||||||
chr3:42694471
|
G | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0096others(6): Show | 13 | HG01070.hp1 HG01175.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1047-653C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694471 | ||||||
chr3:42694538
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047-720G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694538 | ||||||
chr3:42694665
|
C | T | 1 | a0001c0005t0001g0110 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1047-847G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694665 | ||||||
chr3:42694704
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1047-886T>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694704 | ||||||
chr3:42694706
|
G | A | 3 | a0001c0001t0001g0026a0001c0006t0001g0041a0001c0006t0001g0046 | 4 | NA18941.hp1 NA18992.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-888C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694706 | ||||||
chr3:42694813
|
C | T | 1 | a0001c0001t0001g0015 | 5 | HG00621.hp1 NA18947.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-995G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694813 | ||||||
chr3:42694909
|
T | C | 1 | a0001c0006t0001g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1047-1091A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694909 | ||||||
chr3:42694943
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0052a0001c0001t0001g0057others(1): Show | 5 | HG02559.hp2 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1125T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42694943 | ||||||
chr3:42695001
|
GTGCCTAG others(5): Show |
G | 2 | a0002c0004t0001g0022a0002c0004t0001g0071 | 4 | HG02615.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-1195_1047-118 others(16): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695001 | ||||||
chr3:42695165
|
C | A | 10 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0014others(7): Show | 31 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1047-1347G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695165 | ||||||
chr3:42695227
|
C | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1047-1409G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695227 | ||||||
chr3:42695293
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047-1475C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695293 | ||||||
chr3:42695492
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0097a0003c0007t0001g0050others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+1350G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695492 | ||||||
chr3:42695537
|
T | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0038others(5): Show | 15 | HG00639.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046+1305A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695537 | ||||||
chr3:42695537
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(89): Show | 319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1046+1305A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695537 | ||||||
chr3:42695545
|
C | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(59): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1046+1297G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695545 | ||||||
chr3:42695553
|
A | G | 1 | a0002c0003t0001g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1046+1289T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695553 | ||||||
chr3:42695749
|
C | T | 11 | a0002c0002t0001g0005a0002c0002t0001g0010a0002c0002t0001g0040others(8): Show | 53 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1046+1093G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695749 | ||||||
chr3:42695754
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(96): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1046+1088A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695754 | ||||||
chr3:42695989
|
C | T | 1 | a0002c0002t0001g0018 | 4 | HG02109.hp1 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046+853G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42695989 | ||||||
chr3:42696249
|
G | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0075a0001c0008t0001g0029 | 5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+593C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696249 | ||||||
chr3:42696305
|
G | A | 23 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0057others(20): Show | 51 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1046+537C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696305 | ||||||
chr3:42696387
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(69): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1046+455G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696387 | ||||||
chr3:42696509
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1046+333G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696509 | ||||||
chr3:42696535
|
C | T | 2 | a0001c0001t0001g0038a0011c0021t0001g0112 | 3 | HG03209.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1046+307G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696535 | ||||||
chr3:42696547
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(96): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1046+295G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696547 | ||||||
chr3:42696644
|
C | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1046+198G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696644 | ||||||
chr3:42696651
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1046+191G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696651 | ||||||
chr3:42696805
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(42): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1046+37C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 9/11 | chr3 | 42696805 | ||||||
chr3:42696898
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1011-21C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/11 | chr3 | 42696898 | ||||||
chr3:42696978
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1010+23G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 8/11 | chr3 | 42696978 | ||||||
chr3:42697299
|
TG | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0042 | 4 | NA19064.hp2 NA19067.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-155delC | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697299 | ||||||
chr3:42697310
|
C | T | 5 | a0002c0004t0001g0012a0002c0004t0001g0022a0002c0004t0001g0031others(2): Show | 13 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.866-165G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697310 | ||||||
chr3:42697317
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0044others(1): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.866-172A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697317 | ||||||
chr3:42697320
|
T | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0044others(1): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.866-175A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697320 | ||||||
chr3:42697336
|
G | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.865+172C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697336 | ||||||
chr3:42697337
|
A | G | 1 | a0001c0001t0001g0021 | 4 | HG03139.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+171T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697337 | ||||||
chr3:42697342
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0044others(1): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+166C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697342 | ||||||
chr3:42697389
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0044others(1): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+119G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697389 | ||||||
chr3:42697414
|
G | T | 1 | a0002c0004t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+94C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697414 | ||||||
chr3:42697440
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0075a0001c0008t0001g0029 | 5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+68C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697440 | ||||||
chr3:42697443
|
G | A | 1 | a0002c0002t0001g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.865+65C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697443 | ||||||
chr3:42697471
|
C | T | 5 | a0002c0004t0001g0012a0002c0004t0001g0022a0002c0004t0001g0031others(2): Show | 13 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.865+37G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697471 | ||||||
chr3:42697472
|
G | A | 1 | a0002c0011t0001g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.865+36C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697472 | ||||||
chr3:42697496
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.865+12G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 7/11 | chr3 | 42697496 | ||||||
chr3:42697724
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.694-45C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697724 | ||||||
chr3:42697755
|
T | C | 39 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0038others(36): Show | 79 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.694-76A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697755 | ||||||
chr3:42697794
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.694-115G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697794 | ||||||
chr3:42697854
|
G | A | 5 | a0002c0004t0001g0012a0002c0004t0001g0022a0002c0004t0001g0031others(2): Show | 13 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.694-175C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697854 | ||||||
chr3:42697906
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0057others(11): Show | 24 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.694-227C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42697906 | ||||||
chr3:42698030
|
A | G | 1 | a0003c0007t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.693+112T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 6/11 | chr3 | 42698030 | ||||||
chr3:42698458
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0092 | 3 | HG01243.hp1 HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.484-107G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698458 | ||||||
chr3:42698459
|
C | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0044others(1): Show | 10 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-108G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698459 | ||||||
chr3:42698467
|
C | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.484-116G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698467 | ||||||
chr3:42698533
|
GA | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.483+174delT | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698533 | ||||||
chr3:42698545
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.483+163A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 5/11 | chr3 | 42698545 | ||||||
chr3:42698922
|
T | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0115 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.289-20A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/11 | chr3 | 42698922 | ||||||
chr3:42698942
|
G | A | 1 | a0002c0002t0001g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.289-40C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/11 | chr3 | 42698942 | ||||||
chr3:42699000
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 14 | HG00280.hp2 HG01074.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.288+32C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 4/11 | chr3 | 42699000 | ||||||
chr3:42699204
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.175-59G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699204 | ||||||
chr3:42699289
|
T | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0044 | 8 | HG00639.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-144A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699289 | ||||||
chr3:42699325
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0075a0001c0008t0001g0029 | 5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-180G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699325 | ||||||
chr3:42699325
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.175-180G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699325 | ||||||
chr3:42699368
|
C | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0058others(17): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.175-223G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699368 | ||||||
chr3:42699436
|
G | T | 4 | a0001c0006t0001g0027a0001c0006t0001g0046a0001c0006t0001g0047others(1): Show | 5 | HG01891.hp2 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-291C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699436 | ||||||
chr3:42699443
|
C | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.175-298G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699443 | ||||||
chr3:42699734
|
G | GACCCTGG others(17): Show |
1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.174_174+23dupGGTAG others(19): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699734 | ||||||
chr3:42699743
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.174+15T>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 3/11 | chr3 | 42699743 | ||||||
chr3:42699903
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.107-78G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42699903 | ||||||
chr3:42700006
|
C | CTG | 3 | a0001c0001t0001g0026a0001c0006t0001g0041a0002c0002t0001g0014 | 8 | NA18941.hp1 NA18964.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-183_107-182dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700006 | ||||||
chr3:42700020
|
G | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(38): Show | 186 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.107-195C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700020 | ||||||
chr3:42700080
|
C | CTG | 23 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0038others(20): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.107-257_107-256dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700080 | ||||||
chr3:42700080
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.107-255G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700080 | ||||||
chr3:42700082
|
G | C | 4 | a0001c0006t0001g0027a0001c0006t0001g0046a0001c0006t0001g0047others(1): Show | 5 | HG01891.hp2 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-257C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700082 | ||||||
chr3:42700096
|
G | C | 3 | a0002c0002t0001g0009a0002c0002t0001g0043a0010c0018t0001g0055 | 9 | HG01123.hp1 HG01975.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-271C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700096 | ||||||
chr3:42700118
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-293T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700118 | ||||||
chr3:42700122
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-297G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700122 | ||||||
chr3:42700124
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-299C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700124 | ||||||
chr3:42700128
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-303G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700128 | ||||||
chr3:42700134
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-309G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700134 | ||||||
chr3:42700135
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-310A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700135 | ||||||
chr3:42700136
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-311G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700136 | ||||||
chr3:42700137
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-312A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700137 | ||||||
chr3:42700141
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-316A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700141 | ||||||
chr3:42700142
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-317C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700142 | ||||||
chr3:42700143
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-318A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700143 | ||||||
chr3:42700149
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-324A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700149 | ||||||
chr3:42700150
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-325G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700150 | ||||||
chr3:42700156
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-331G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700156 | ||||||
chr3:42700158
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-333T>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700158 | ||||||
chr3:42700163
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-338A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700163 | ||||||
chr3:42700164
|
C | CTG | 19 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0058others(16): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.107-341_107-340dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | ||||||
chr3:42700164
|
C | CTGTG | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0006t0001g0027others(5): Show | 11 | HG00323.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-343_107-340dup others(4): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | ||||||
chr3:42700164
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-339G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | ||||||
chr3:42700164
|
CTG | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(46): Show | 198 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.107-341_107-340del others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700164 | ||||||
chr3:42700182
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-357C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700182 | ||||||
chr3:42700183
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-358A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700183 | ||||||
chr3:42700185
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-360A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700185 | ||||||
chr3:42700196
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-371C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700196 | ||||||
chr3:42700200
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-375C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700200 | ||||||
chr3:42700201
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-376A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700201 | ||||||
chr3:42700206
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-381T>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700206 | ||||||
chr3:42700208
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-383T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700208 | ||||||
chr3:42700212
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-387G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700212 | ||||||
chr3:42700236
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-411T>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700236 | ||||||
chr3:42700237
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-412A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700237 | ||||||
chr3:42700239
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-414G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700239 | ||||||
chr3:42700250
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-425G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700250 | ||||||
chr3:42700251
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-426A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700251 | ||||||
chr3:42700253
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0102 | 3 | HG01070.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107-428A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700253 | ||||||
chr3:42700261
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-436A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700261 | ||||||
chr3:42700262
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-437C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700262 | ||||||
chr3:42700263
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.107-438A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700263 | ||||||
chr3:42700266
|
GGGTCCAG others(3): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+445_107-442del others(10): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700266 | ||||||
chr3:42700283
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+438A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700283 | ||||||
chr3:42700284
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+437C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700284 | ||||||
chr3:42700287
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+434A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700287 | ||||||
chr3:42700288
|
A | ATG | 3 | a0001c0001t0001g0024a0001c0001t0001g0079a0002c0002t0001g0053 | 5 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+431_106+432dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700288 | ||||||
chr3:42700288
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+433T>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700288 | ||||||
chr3:42700293
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+428A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700293 | ||||||
chr3:42700294
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+427C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700294 | ||||||
chr3:42700300
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.106+421C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700300 | ||||||
chr3:42700301
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+420A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700301 | ||||||
chr3:42700310
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+411C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700310 | ||||||
chr3:42700318
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+403C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700318 | ||||||
chr3:42700345
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.106+376A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700345 | ||||||
chr3:42700346
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+375G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700346 | ||||||
chr3:42700360
|
CTG | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0026others(46): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.106+359_106+360del others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700360 | ||||||
chr3:42700380
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+341G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700380 | ||||||
chr3:42700387
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+334A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700387 | ||||||
chr3:42700392
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+329C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700392 | ||||||
chr3:42700398
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+323T>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700398 | ||||||
chr3:42700402
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+319G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700402 | ||||||
chr3:42700405
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+316C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700405 | ||||||
chr3:42700412
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+309C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700412 | ||||||
chr3:42700415
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+306A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700415 | ||||||
chr3:42700416
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+305G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700416 | ||||||
chr3:42700417
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+304A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700417 | ||||||
chr3:42700418
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+303C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700418 | ||||||
chr3:42700421
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+300A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700421 | ||||||
chr3:42700429
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+292A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700429 | ||||||
chr3:42700437
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+284G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700437 | ||||||
chr3:42700439
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+282C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700439 | ||||||
chr3:42700442
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+279G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700442 | ||||||
chr3:42700443
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+278A>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700443 | ||||||
chr3:42700444
|
C | CTG | 5 | a0001c0001t0001g0023a0001c0012t0001g0032a0001c0019t0001g0078others(2): Show | 10 | HG01070.hp1 HG01175.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+275_106+276dup others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700444 | ||||||
chr3:42700444
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+277G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700444 | ||||||
chr3:42700444
|
CTG | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0026others(46): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.106+275_106+276del others(2): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700444 | ||||||
chr3:42700462
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.106+259C>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700462 | ||||||
chr3:42700623
|
G | T | 1 | a0002c0004t0002g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.106+98C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700623 | ||||||
chr3:42700645
|
G | A | 1 | a0001c0001t0001g0020 | 4 | HG01074.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+76C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700645 | ||||||
chr3:42700659
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.106+62C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700659 | ||||||
chr3:42700664
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.106+57G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 2/11 | chr3 | 42700664 | ||||||
chr3:42700874
|
T | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0057 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-13-35A>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42700874 | ||||||
chr3:42700876
|
C | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-13-37G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42700876 | ||||||
chr3:42700913
|
C | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-13-74G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42700913 | ||||||
chr3:42701015
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0103 | 3 | HG01257.hp1 HG01258.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-13-176C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701015 | ||||||
chr3:42701027
|
C | T | 1 | a0001c0005t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-13-188G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701027 | ||||||
chr3:42701078
|
C | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-13-239G>C | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701078 | ||||||
chr3:42701146
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0039others(20): Show | 79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-13-307C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701146 | ||||||
chr3:42701199
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-13-360C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701199 | ||||||
chr3:42701239
|
T | C | 1 | a0001c0001t0001g0006 | 10 | HG01496.hp1 HG01928.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-400A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701239 | ||||||
chr3:42701240
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-13-401C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701240 | ||||||
chr3:42701256
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02145.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-13-417C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701256 | ||||||
chr3:42701398
|
C | A | 1 | a0001c0001t0001g0016 | 5 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-559G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701398 | ||||||
chr3:42701575
|
T | TGGGGCCA others(3): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0104others(4): Show | 39 | HG00621.hp1 HG01081.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.-13-746_-13-737dup others(10): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701575 | ||||||
chr3:42701575
|
TGGGGCCA others(3): Show |
T | 4 | a0001c0001t0001g0026a0001c0001t0001g0076a0001c0006t0001g0041others(1): Show | 5 | HG02809.hp2 NA18941.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-746_-13-737del others(10): Show |
HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701575 | ||||||
chr3:42701649
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0075a0001c0008t0001g0029 | 5 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-810G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701649 | ||||||
chr3:42701652
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0016others(49): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-13-813G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701652 | ||||||
chr3:42701702
|
C | A | 1 | a0001c0001t0001g0108 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-13-863G>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701702 | ||||||
chr3:42701962
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-14+617G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701962 | ||||||
chr3:42701983
|
G | T | 2 | a0001c0001t0001g0026a0001c0006t0001g0041 | 3 | NA18941.hp1 NA18992.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-14+596C>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42701983 | ||||||
chr3:42702053
|
G | A | 4 | a0001c0005t0001g0007a0001c0005t0001g0109a0001c0005t0001g0110others(1): Show | 13 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14+526C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702053 | ||||||
chr3:42702091
|
T | C | 1 | a0004c0010t0001g0037 | 2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-14+488A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702091 | ||||||
chr3:42702259
|
T | C | 2 | a0001c0001t0001g0038a0011c0021t0001g0112 | 3 | HG03209.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-14+320A>G | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702259 | ||||||
chr3:42702366
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02145.hp1 HG03471.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+213C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702366 | ||||||
chr3:42702375
|
C | T | 1 | a0002c0002t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-14+204G>A | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702375 | ||||||
chr3:42702476
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0039 | 7 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+103C>T | HHATL | ENSG00000010282.15 | transcript | ENST00000441594.6 | protein_coding | 1/11 | chr3 | 42702476 |