geneid | 55363 |
---|---|
ensemblid | ENSG00000136929.13 |
hgncid | 17509 |
symbol | HEMGN |
name | hemogen |
refseq_nuc | NM_197978.3 |
refseq_prot | NP_932095.1 |
ensembl_nuc | ENST00000616898.2 |
ensembl_prot | ENSP00000480020.1 |
mane_status | MANE Select |
chr | chr9 |
start | 97926791 |
end | 97938172 |
strand | - |
ver | v1.2 |
region | chr9:97926791-97938172 |
region5000 | chr9:97921791-97943172 |
regionname0 | HEMGN_chr9_97926791_97938172 |
regionname5000 | HEMGN_chr9_97921791_97943172 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 484 | 312 | 64 | 62 | 127 | 16 | 41 | 93 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0002 | 0/0 | 484 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0003 | 0/0 | 484 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1455 | 282 | 62 | 48 | 123 | 15 | 32 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
c0002 | 0/0 | 1455 | 27 | 2 | 14 | 2 | 0 | 9 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
c0003 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
c0004 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
c0005 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
c0006 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 628 | 134 | 30 | 15 | 69 | 4 | 16 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
t0002 | 1/1 | 630 | 94 | 18 | 19 | 36 | 7 | 12 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
t0003 | 0/0 | 622 | 72 | 4 | 27 | 22 | 5 | 14 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
t0004 | 0/0 | 624 | 5 | 4 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
t0005 | 0/0 | 622 | 4 | 3 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
t0006 | 0/0 | 630 | 4 | 4 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
t0007 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
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 | 88 | 19 | 12 | 46 | 3 | 8 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0002 | 1/1 | 56 | 11 | 14 | 20 | 3 | 6 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0003 | 0/0 | 20 | 0 | 6 | 11 | 1 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0004 | 0/0 | 15 | 1 | 7 | 1 | 0 | 6 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0005 | 0/0 | 10 | 3 | 2 | 4 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0006 | 0/0 | 9 | 0 | 4 | 0 | 3 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0009 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1455 | 282 | 62 | 48 | 123 | 15 | 32 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0002 | 0/0 | 1455 | 27 | 2 | 14 | 2 | 0 | 9 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0003 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0005 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0002c0004 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0003c0006 | 0/0 | 1455 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2082 | 130 | 30 | 15 | 66 | 4 | 15 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0001t0002 | 1/1 | 2084 | 93 | 18 | 19 | 36 | 6 | 12 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0001t0003 | 0/0 | 2076 | 46 | 3 | 13 | 20 | 5 | 5 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0001t0004 | 0/0 | 2078 | 4 | 3 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0001t0005 | 0/0 | 2076 | 4 | 3 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0001t0006 | 0/0 | 2084 | 4 | 4 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0001t0007 | 0/0 | 2084 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0002t0003 | 0/0 | 2076 | 26 | 1 | 14 | 2 | 0 | 9 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0002t0004 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0003t0001 | 0/0 | 2082 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0001c0005t0002 | 0/0 | 2084 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0002c0004t0001 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
a0003c0006t0001 | 0/0 | 2082 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | copy fasta | chr9 | 97921791 | 97943172 |
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 | 88 | 19 | 12 | 46 | 3 | 8 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0005 | 0/0 | 10 | 3 | 2 | 4 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0002 | 1/1 | 56 | 11 | 14 | 20 | 3 | 6 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0003 | 0/0 | 20 | 0 | 6 | 11 | 1 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0006 | 0/0 | 9 | 0 | 4 | 0 | 3 | 2 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0005g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0004 | 0/0 | 15 | 1 | 7 | 1 | 0 | 6 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0002t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0001c0005t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0002c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
a0003c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00323 | hp1 | a0001 | c0005 | t0002 | g0059 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0079 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0035 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01993 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0081 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03710 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0083 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03942 | hp2 | a0003 | c0006 | t0001 | g0056 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0080 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04228 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0076 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19066 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19089 | hp2 | a0002 | c0004 | t0001 | g0063 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ASW | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | TSI | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | GIH | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | USA | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | LWK | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0002 | REF | REF | HEMGN_chr9_97921791_97943172 | HEMGN | chr9 | 97921791 | 97943172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97930754
|
T | C | 1 | a0002 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.641A>G | p.His214Arg | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 677/2084 | 641/1455 | 214/484 | chr9 | 97930754 | ||
chr9:97930800
|
C | A | 1 | a0003 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.595G>T | p.Asp199Tyr | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 631/2084 | 595/1455 | 199/484 | chr9 | 97930800 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97927411
|
A | G | 1 | a0001c0002 | 27 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
synonymous_variant | LOW | c.1428T>C | p.Asn476Asn | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 1464/2084 | 1428/1455 | 476/484 | chr9 | 97927411 | ||
chr9:97930366
|
G | T | 1 | a0001c0005 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1029C>A | p.Ile343Ile | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 1065/2084 | 1029/1455 | 343/484 | chr9 | 97930366 | ||
chr9:97931145
|
A | G | 2 | a0001c0003a0002c0004 | 3 | NA18947.hp2 NA18981.hp1 NA19089.hp2 |
synonymous_variant | LOW | c.250T>C | p.Leu84Leu | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/4 | 286/2084 | 250/1455 | 84/484 | chr9 | 97931145 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97927093
|
A | T | 1 | a0001c0001t0005 | 4 | HG01243.hp1 HG01891.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*291T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 291 | chr9 | 97927093 | |||||
chr9:97927168
|
TAC | T | 4 | a0001c0001t0001a0001c0003t0001a0002c0004t0001others(1): Show | 134 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*214_*215delGT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 214 | chr9 | 97927168 | |||||
chr9:97927168
|
TACACAC | T | 2 | a0001c0001t0004a0001c0002t0004 | 5 | HG02818.hp2 HG02886.hp1 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*210_*215delGTGTGT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 210 | chr9 | 97927168 | |||||
chr9:97927168
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0003a0001c0001t0005a0001c0002t0003 | 76 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*208_*215delGTGTGT others(2): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 208 | chr9 | 97927168 | |||||
chr9:97927250
|
T | G | 1 | a0001c0001t0007 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 134 | chr9 | 97927250 | |||||
chr9:97927260
|
G | A | 2 | a0001c0001t0006a0001c0001t0007 | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*124C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 4/4 | 124 | chr9 | 97927260 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97927585
|
C | T | 1 | a0001c0001t0004g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1361-107G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97927585 | ||||||
chr9:97927635
|
G | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0069 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1361-157C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97927635 | ||||||
chr9:97927902
|
T | G | 1 | a0001c0001t0004g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1361-424A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97927902 | ||||||
chr9:97928025
|
A | AT | 14 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0002g0015others(11): Show | 20 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1361-548dupA | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | ||||||
chr9:97928025
|
A | ATT | 7 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0027others(4): Show | 15 | HG00597.hp1 HG00642.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-549_1361-548d others(4): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | ||||||
chr9:97928025
|
A | T | 1 | a0001c0001t0006g0026 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1361-547T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | ||||||
chr9:97928025
|
AT | A | 11 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0011others(8): Show | 42 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-548delA | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928025 | ||||||
chr9:97928079
|
T | G | 1 | a0001c0001t0006g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-601A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928079 | ||||||
chr9:97928125
|
C | G | 1 | a0001c0001t0002g0015 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1361-647G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928125 | ||||||
chr9:97928239
|
A | G | 1 | a0001c0001t0001g0010 | 4 | NA18944.hp2 NA18955.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-761T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928239 | ||||||
chr9:97928242
|
G | T | 2 | a0001c0001t0004g0034a0001c0001t0004g0084 | 2 | HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1361-764C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928242 | ||||||
chr9:97928273
|
A | G | 32 | a0001c0001t0002g0048a0001c0001t0002g0066a0001c0001t0003g0003others(29): Show | 82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1361-795T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928273 | ||||||
chr9:97928342
|
T | C | 1 | a0001c0001t0003g0014 | 2 | NA18961.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1361-864A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928342 | ||||||
chr9:97928699
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1361-1221A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928699 | ||||||
chr9:97928736
|
G | T | 1 | a0001c0001t0002g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1361-1258C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928736 | ||||||
chr9:97928816
|
A | G | 1 | a0001c0001t0001g0025 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1360+1219T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928816 | ||||||
chr9:97928857
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1360+1178A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928857 | ||||||
chr9:97928886
|
G | A | 32 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(29): Show | 82 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1360+1149C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928886 | ||||||
chr9:97928916
|
A | G | 1 | a0003c0006t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1360+1119T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97928916 | ||||||
chr9:97929115
|
C | T | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1360+920G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929115 | ||||||
chr9:97929138
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1360+897T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929138 | ||||||
chr9:97929482
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1360+553C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929482 | ||||||
chr9:97929618
|
T | TG | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1360+416_1360+417i others(3): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929618 | ||||||
chr9:97929620
|
A | G | 1 | a0001c0001t0003g0045 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1360+415T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929620 | ||||||
chr9:97929648
|
T | G | 1 | a0001c0001t0006g0074 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1360+387A>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929648 | ||||||
chr9:97929827
|
G | A | 5 | a0001c0001t0002g0048a0001c0001t0006g0026a0001c0001t0006g0074others(2): Show | 6 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+208C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929827 | ||||||
chr9:97929955
|
T | TA | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1360+79dupT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 3/3 | chr9 | 97929955 | ||||||
chr9:97931298
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.174-77G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931298 | ||||||
chr9:97931427
|
A | G | 1 | a0001c0001t0004g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.174-206T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931427 | ||||||
chr9:97931435
|
G | C | 9 | a0001c0002t0003g0004a0001c0002t0003g0008a0001c0002t0003g0035others(6): Show | 27 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.174-214C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931435 | ||||||
chr9:97931574
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.174-353C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931574 | ||||||
chr9:97931783
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.174-562T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97931783 | ||||||
chr9:97932365
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.174-1144A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932365 | ||||||
chr9:97932676
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.174-1455G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932676 | ||||||
chr9:97932677
|
G | A | 1 | a0001c0002t0003g0083 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174-1456C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932677 | ||||||
chr9:97932727
|
C | T | 4 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0085others(1): Show | 11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.174-1506G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932727 | ||||||
chr9:97932739
|
G | T | 1 | a0001c0002t0003g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.174-1518C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932739 | ||||||
chr9:97932803
|
C | CAAAA | 17 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(14): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.174-1586_174-1583d others(6): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932803 | ||||||
chr9:97932803
|
C | CAAAAA | 11 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0003g0047others(8): Show | 29 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.174-1587_174-1583d others(7): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932803 | ||||||
chr9:97932803
|
CA | C | 6 | a0001c0001t0001g0060a0001c0001t0002g0020a0001c0001t0002g0085others(3): Show | 8 | HG00323.hp1 HG01517.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.174-1583delT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932803 | ||||||
chr9:97932930
|
A | T | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.174-1709T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932930 | ||||||
chr9:97932973
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.174-1752A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97932973 | ||||||
chr9:97933007
|
T | C | 1 | a0001c0001t0006g0026 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.174-1786A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933007 | ||||||
chr9:97933114
|
T | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0085others(1): Show | 11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.174-1893A>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933114 | ||||||
chr9:97933494
|
T | C | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.174-2273A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933494 | ||||||
chr9:97933502
|
C | T | 4 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0085others(1): Show | 11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.174-2281G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933502 | ||||||
chr9:97933511
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.174-2290T>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933511 | ||||||
chr9:97933618
|
C | T | 2 | a0001c0001t0001g0055a0003c0006t0001g0056 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.174-2397G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933618 | ||||||
chr9:97933619
|
G | A | 40 | a0001c0001t0001g0043a0001c0001t0002g0007a0001c0001t0002g0027others(37): Show | 97 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.174-2398C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933619 | ||||||
chr9:97933726
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.173+2445G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933726 | ||||||
chr9:97933921
|
T | C | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.173+2250A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933921 | ||||||
chr9:97933986
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.173+2185C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97933986 | ||||||
chr9:97934117
|
T | C | 1 | a0001c0001t0004g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173+2054A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934117 | ||||||
chr9:97934354
|
G | A | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.173+1817C>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934354 | ||||||
chr9:97934384
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0052 | 3 | HG00642.hp2 HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.173+1787T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934384 | ||||||
chr9:97934392
|
A | AAGGAGAG others(3): Show |
13 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(10): Show | 43 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.173+1769_173+1778d others(12): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934392 | ||||||
chr9:97934404
|
G | C | 4 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0085others(1): Show | 11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.173+1767C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934404 | ||||||
chr9:97934435
|
AGGGGGAG others(10): Show |
A | 1 | a0001c0001t0001g0025 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.173+1719_173+1735d others(19): Show |
HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934435 | ||||||
chr9:97934451
|
A | AG | 15 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0002g0019others(12): Show | 28 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.173+1719dupC | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934451 | ||||||
chr9:97934453
|
G | T | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.173+1718C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934453 | ||||||
chr9:97934458
|
A | G | 1 | a0001c0001t0003g0042 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.173+1713T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934458 | ||||||
chr9:97934518
|
A | G | 5 | a0001c0001t0002g0048a0001c0001t0006g0026a0001c0001t0006g0074others(2): Show | 6 | HG02451.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+1653T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934518 | ||||||
chr9:97934989
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.173+1182C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97934989 | ||||||
chr9:97935005
|
A | G | 31 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(28): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.173+1166T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935005 | ||||||
chr9:97935048
|
C | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0052 | 3 | HG00642.hp2 HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.173+1123G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935048 | ||||||
chr9:97935101
|
C | A | 1 | a0001c0001t0004g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.173+1070G>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935101 | ||||||
chr9:97935111
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.173+1060C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935111 | ||||||
chr9:97935192
|
A | G | 1 | a0001c0001t0003g0042 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.173+979T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935192 | ||||||
chr9:97935366
|
T | A | 41 | a0001c0001t0001g0043a0001c0001t0002g0007a0001c0001t0002g0015others(38): Show | 99 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.173+805A>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935366 | ||||||
chr9:97935730
|
C | T | 1 | a0001c0001t0003g0041 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.173+441G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935730 | ||||||
chr9:97935865
|
A | G | 9 | a0001c0002t0003g0004a0001c0002t0003g0008a0001c0002t0003g0035others(6): Show | 27 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.173+306T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97935865 | ||||||
chr9:97936079
|
T | C | 4 | a0001c0001t0004g0034a0001c0001t0005g0013a0001c0001t0005g0039others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.173+92A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97936079 | ||||||
chr9:97936091
|
T | C | 1 | a0001c0001t0004g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.173+80A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97936091 | ||||||
chr9:97936142
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.173+29C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 2/3 | chr9 | 97936142 | ||||||
chr9:97936353
|
C | G | 1 | a0001c0001t0001g0017 | 2 | NA18951.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.80-89G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936353 | ||||||
chr9:97936401
|
T | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0085others(1): Show | 11 | NA18943.hp1 NA18944.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-137A>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936401 | ||||||
chr9:97936895
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.80-631G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936895 | ||||||
chr9:97936956
|
C | A | 13 | a0001c0001t0001g0043a0001c0001t0002g0044a0001c0001t0003g0003others(10): Show | 43 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.80-692G>T | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936956 | ||||||
chr9:97936960
|
T | C | 35 | a0001c0001t0001g0043a0001c0001t0002g0007a0001c0001t0002g0027others(32): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.80-696A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97936960 | ||||||
chr9:97937061
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.80-797G>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937061 | ||||||
chr9:97937074
|
G | C | 1 | a0001c0001t0002g0015 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.80-810C>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937074 | ||||||
chr9:97937081
|
C | T | 1 | a0001c0001t0002g0015 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.80-817G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937081 | ||||||
chr9:97937328
|
A | G | 1 | a0001c0001t0002g0012 | 3 | HG03704.hp2 HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.79+730T>C | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937328 | ||||||
chr9:97937479
|
G | T | 1 | a0001c0001t0002g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+579C>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937479 | ||||||
chr9:97937488
|
C | T | 1 | a0001c0001t0004g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+570G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937488 | ||||||
chr9:97937548
|
A | C | 35 | a0001c0001t0001g0043a0001c0001t0002g0007a0001c0001t0002g0027others(32): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+510T>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937548 | ||||||
chr9:97937670
|
C | T | 1 | a0001c0001t0004g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+388G>A | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937670 | ||||||
chr9:97937698
|
TA | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0032a0001c0001t0003g0033 | 11 | HG00280.hp1 HG00735.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+359delT | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937698 | ||||||
chr9:97937875
|
T | C | 35 | a0001c0001t0001g0043a0001c0001t0002g0007a0001c0001t0002g0027others(32): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+183A>G | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937875 | ||||||
chr9:97937960
|
C | CT | 26 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0002g0028others(23): Show | 61 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.79+97dupA | HEMGN | ENSG00000136929.13 | transcript | ENST00000616898.2 | protein_coding | 1/3 | chr9 | 97937960 |