geneid | 3067 |
---|---|
ensemblid | ENSG00000140287.11 |
hgncid | 4855 |
symbol | HDC |
name | histidine decarboxylase |
refseq_nuc | NM_002112.4 |
refseq_prot | NP_002103.2 |
ensembl_nuc | ENST00000267845.8 |
ensembl_prot | ENSP00000267845.3 |
mane_status | MANE Select |
chr | chr15 |
start | 50241947 |
end | 50265726 |
strand | - |
ver | v1.2 |
region | chr15:50241947-50265726 |
region5000 | chr15:50236947-50270726 |
regionname0 | HDC_chr15_50241947_50265726 |
regionname5000 | HDC_chr15_50236947_50270726 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 662 | 362 | 78 | 64 | 155 | 16 | 47 | 120 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002 | 0/0 | 662 | 30 | 10 | 4 | 14 | 2 | 0 | 9 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0003 | 0/0 | 662 | 18 | 0 | 8 | 9 | 0 | 1 | 5 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0004 | 0/0 | 662 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0005 | 0/0 | 662 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1989 | 338 | 57 | 64 | 152 | 16 | 47 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0002 | 0/0 | 1989 | 20 | 6 | 0 | 14 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0003 | 0/0 | 1989 | 18 | 0 | 8 | 9 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0004 | 0/0 | 1989 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0005 | 0/0 | 1989 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0006 | 0/0 | 1989 | 7 | 6 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0007 | 0/0 | 1989 | 7 | 1 | 4 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0008 | 0/0 | 1989 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0009 | 0/0 | 1989 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0010 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0011 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
c0012 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 417 | 382 | 75 | 75 | 164 | 18 | 48 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
t0002 | 0/0 | 417 | 34 | 19 | 1 | 14 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
t0003 | 0/0 | 417 | 2 | 0 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 0 | 2 | 19 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0002 | 0/0 | 14 | 1 | 4 | 9 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0003 | 0/0 | 14 | 0 | 5 | 3 | 1 | 5 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0004 | 0/0 | 13 | 10 | 0 | 2 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0005 | 0/0 | 13 | 0 | 2 | 6 | 2 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0006 | 0/0 | 11 | 3 | 3 | 0 | 3 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0007 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0008 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0009 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0014 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0018 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0020 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0029 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0042 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0045 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0056 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1989 | 338 | 57 | 64 | 152 | 16 | 47 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0004 | 0/0 | 1989 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0005 | 0/0 | 1989 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0009 | 0/0 | 1989 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0010 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0012 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002c0002 | 0/0 | 1989 | 20 | 6 | 0 | 14 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002c0007 | 0/0 | 1989 | 7 | 1 | 4 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002c0008 | 0/0 | 1989 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0003c0003 | 0/0 | 1989 | 18 | 0 | 8 | 9 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0004c0006 | 0/0 | 1989 | 7 | 6 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0005c0011 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2405 | 336 | 57 | 62 | 152 | 16 | 47 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0001t0003 | 0/0 | 2405 | 2 | 0 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0004t0001 | 0/0 | 2405 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0005t0001 | 0/0 | 2405 | 6 | 6 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0005t0002 | 0/0 | 2405 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0009t0001 | 0/0 | 2405 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0010t0001 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0001c0012t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002c0002t0002 | 0/0 | 2405 | 20 | 6 | 0 | 14 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002c0007t0001 | 0/0 | 2405 | 7 | 1 | 4 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0002c0008t0002 | 0/0 | 2405 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0003c0003t0001 | 0/0 | 2405 | 18 | 0 | 8 | 9 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0004c0006t0002 | 0/0 | 2405 | 7 | 6 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
a0005c0011t0001 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | copy fasta | chr15 | 50236947 | 50270726 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 0 | 2 | 19 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0002 | 0/0 | 14 | 1 | 4 | 9 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0003 | 0/0 | 14 | 0 | 5 | 3 | 1 | 5 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0004 | 0/0 | 13 | 10 | 0 | 2 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0005 | 0/0 | 13 | 0 | 2 | 6 | 2 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0006 | 0/0 | 11 | 3 | 3 | 0 | 3 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0009 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0014 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0018 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0042 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0045 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0005t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0005t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0005t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0005t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0009t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0010t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0001c0012t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0007t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0007t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0007t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0007t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0008t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0008t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0002c0008t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0020 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0004c0006t0002g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0004c0006t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0004c0006t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0004c0006t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
a0005c0011t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0007 | t0001 | g0061 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0203 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00733 | hp1 | a0002 | c0007 | t0001 | g0059 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01070 | hp1 | a0003 | c0003 | t0001 | g0201 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01071 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01074 | hp2 | a0002 | c0007 | t0001 | g0060 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01099 | hp2 | a0002 | c0007 | t0001 | g0036 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01106 | hp1 | a0003 | c0003 | t0001 | g0199 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01109 | hp2 | a0004 | c0006 | t0002 | g0190 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01168 | hp1 | a0005 | c0011 | t0001 | g0150 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0202 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01891 | hp1 | a0001 | c0005 | t0002 | g0188 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0198 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02056 | hp2 | a0001 | c0009 | t0001 | g0106 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02145 | hp1 | a0004 | c0006 | t0002 | g0021 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02257 | hp2 | a0004 | c0006 | t0002 | g0021 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02451 | hp2 | a0001 | c0005 | t0002 | g0052 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02572 | hp1 | a0001 | c0005 | t0001 | g0057 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0080 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02615 | hp2 | a0001 | c0005 | t0002 | g0195 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02622 | hp2 | a0004 | c0006 | t0002 | g0233 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02647 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0146 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02809 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0142 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02886 | hp2 | a0004 | c0006 | t0002 | g0021 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02922 | hp1 | a0002 | c0008 | t0002 | g0208 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02970 | hp2 | a0001 | c0004 | t0001 | g0196 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02976 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03098 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03195 | hp2 | a0001 | c0012 | t0001 | g0140 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03209 | hp1 | a0004 | c0006 | t0002 | g0021 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03225 | hp2 | a0002 | c0008 | t0002 | g0230 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0204 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18974 | hp2 | a0001 | c0010 | t0001 | g0138 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19000 | hp1 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19001 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19067 | hp1 | a0003 | c0003 | t0001 | g0205 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19077 | hp1 | a0001 | c0009 | t0001 | g0127 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19090 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | ASW | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20752 | hp2 | a0002 | c0007 | t0001 | g0036 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | GIH | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG01123 | hp2 | a0002 | c0007 | t0001 | g0062 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02486 | hp1 | a0002 | c0007 | t0001 | g0232 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03471 | hp1 | a0001 | c0005 | t0002 | g0052 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG03471 | hp2 | a0002 | c0008 | t0002 | g0144 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG06807 | hp1 | a0004 | c0006 | t0002 | g0145 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0156 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0042 | REF | REF | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0108 | REF | REF | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:50242317
|
T | G | 2 | a0002a0004 | 37 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(34): Show |
missense_variant | MODERATE | c.1932A>C | p.Glu644Asp | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 2035/2405 | 1932/1989 | 644/662 | chr15 | 50242317 | ||
chr15:50242592
|
A | G | 1 | a0004 | 7 | HG01109.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
missense_variant | MODERATE | c.1657T>C | p.Phe553Leu | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1760/2405 | 1657/1989 | 553/662 | chr15 | 50242592 | ||
chr15:50242769
|
T | C | 1 | a0005 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1480A>G | p.Ile494Val | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1583/2405 | 1480/1989 | 494/662 | chr15 | 50242769 | ||
chr15:50263347
|
G | A | 1 | a0003 | 18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
missense_variant | MODERATE | c.92C>T | p.Thr31Met | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/12 | 195/2405 | 92/1989 | 31/662 | chr15 | 50263347 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:50242479
|
C | T | 1 | a0001c0004 | 10 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(7): Show |
synonymous_variant | LOW | c.1770G>A | p.Val590Val | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1873/2405 | 1770/1989 | 590/662 | chr15 | 50242479 | ||
chr15:50242506
|
C | T | 1 | a0002c0002 | 20 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(17): Show |
synonymous_variant | LOW | c.1743G>A | p.Thr581Thr | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1846/2405 | 1743/1989 | 581/662 | chr15 | 50242506 | ||
chr15:50242635
|
A | G | 6 | a0001c0004a0001c0005a0002c0002others(3): Show | 57 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
synonymous_variant | LOW | c.1614T>C | p.Asn538Asn | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1717/2405 | 1614/1989 | 538/662 | chr15 | 50242635 | ||
chr15:50242842
|
A | G | 1 | a0001c0009 | 2 | HG02056.hp2 NA19077.hp1 |
synonymous_variant | LOW | c.1407T>C | p.Asp469Asp | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1510/2405 | 1407/1989 | 469/662 | chr15 | 50242842 | ||
chr15:50252674
|
G | A | 1 | a0002c0007 | 7 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(4): Show |
synonymous_variant | LOW | c.888C>T | p.Ala296Ala | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 8/12 | 991/2405 | 888/1989 | 296/662 | chr15 | 50252674 | ||
chr15:50254545
|
G | A | 1 | a0001c0012 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.561C>T | p.Ala187Ala | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 5/12 | 664/2405 | 561/1989 | 187/662 | chr15 | 50254545 | ||
chr15:50263331
|
A | T | 1 | a0001c0010 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.108T>A | p.Pro36Pro | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/12 | 211/2405 | 108/1989 | 36/662 | chr15 | 50263331 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:50242182
|
A | G | 1 | a0001c0001t0003 | 2 | HG01496.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 78 | chr15 | 50242182 | |||||
chr15:50242257
|
T | G | 4 | a0001c0005t0002a0002c0002t0002a0002c0008t0002others(1): Show | 34 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 3 | chr15 | 50242257 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:50243061
|
C | A | 1 | a0001c0005t0002g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1243-55G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 11/11 | chr15 | 50243061 | ||||||
chr15:50243431
|
C | T | 12 | a0002c0002t0002g0023a0002c0002t0002g0030a0002c0002t0002g0031others(9): Show | 20 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1141-187G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243431 | ||||||
chr15:50243514
|
A | G | 2 | a0002c0002t0002g0032a0002c0002t0002g0177 | 4 | NA18941.hp1 NA18980.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-270T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243514 | ||||||
chr15:50243539
|
G | A | 1 | a0002c0008t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1141-295C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243539 | ||||||
chr15:50243547
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1141-303G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243547 | ||||||
chr15:50243610
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1141-366G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243610 | ||||||
chr15:50243615
|
C | T | 18 | a0002c0002t0002g0023a0002c0002t0002g0030a0002c0002t0002g0031others(15): Show | 29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1141-371G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243615 | ||||||
chr15:50243616
|
G | A | 2 | a0001c0004t0001g0156a0001c0004t0001g0198 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1141-372C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243616 | ||||||
chr15:50243677
|
G | A | 3 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195 | 4 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-433C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243677 | ||||||
chr15:50243707
|
G | A | 18 | a0002c0002t0002g0023a0002c0002t0002g0030a0002c0002t0002g0031others(15): Show | 29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1141-463C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243707 | ||||||
chr15:50243744
|
G | A | 1 | a0002c0002t0002g0101 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1141-500C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243744 | ||||||
chr15:50243871
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1141-627A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243871 | ||||||
chr15:50244031
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1141-787A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244031 | ||||||
chr15:50244155
|
C | T | 21 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195others(18): Show | 33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-911G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244155 | ||||||
chr15:50244161
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1141-917A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244161 | ||||||
chr15:50244241
|
T | C | 21 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195others(18): Show | 33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-997A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244241 | ||||||
chr15:50244283
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1141-1039G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244283 | ||||||
chr15:50244285
|
C | CT | 20 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0048others(17): Show | 25 | HG00642.hp1 HG00673.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141-1042dupA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | ||||||
chr15:50244285
|
CT | C | 32 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(29): Show | 49 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1141-1042delA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | ||||||
chr15:50244285
|
CTTT | C | 6 | a0001c0005t0001g0146a0002c0007t0001g0036a0002c0007t0001g0059others(3): Show | 7 | HG00733.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141-1044_1141-104 others(7): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | ||||||
chr15:50244285
|
CTTTT | C | 19 | a0002c0002t0002g0023a0002c0002t0002g0030a0002c0002t0002g0031others(16): Show | 30 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1141-1045_1141-104 others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | ||||||
chr15:50244285
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0004t0001g0053a0001c0004t0001g0080a0001c0004t0001g0139others(4): Show | 8 | HG02572.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1141-1053_1141-104 others(16): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | ||||||
chr15:50244298
|
T | G | 18 | a0002c0002t0002g0023a0002c0002t0002g0030a0002c0002t0002g0031others(15): Show | 29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1141-1054A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244298 | ||||||
chr15:50244312
|
G | T | 1 | a0001c0005t0002g0188 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-1068C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244312 | ||||||
chr15:50244313
|
A | T | 1 | a0001c0005t0002g0188 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-1069T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244313 | ||||||
chr15:50244318
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1141-1074A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244318 | ||||||
chr15:50244385
|
C | G | 1 | a0001c0004t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1141-1141G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244385 | ||||||
chr15:50244415
|
A | ACCTTCAC others(1): Show |
21 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195others(18): Show | 33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-1179_1141-117 others(12): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244415 | ||||||
chr15:50244422
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0081 | 3 | HG00609.hp2 NA18957.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1141-1178G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244422 | ||||||
chr15:50244615
|
T | C | 1 | a0001c0001t0001g0039 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1141-1371A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244615 | ||||||
chr15:50244646
|
A | T | 10 | a0001c0001t0001g0051a0001c0001t0001g0115a0003c0003t0001g0020others(7): Show | 14 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1141-1402T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244646 | ||||||
chr15:50244678
|
G | C | 1 | a0001c0009t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1141-1434C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244678 | ||||||
chr15:50244985
|
C | T | 21 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195others(18): Show | 33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-1741G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244985 | ||||||
chr15:50245281
|
C | G | 1 | a0003c0003t0001g0019 | 4 | HG02083.hp2 NA19001.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-2037G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245281 | ||||||
chr15:50245281
|
C | T | 21 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195others(18): Show | 33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-2037G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245281 | ||||||
chr15:50245323
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1141-2079C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245323 | ||||||
chr15:50245352
|
C | T | 27 | a0001c0005t0002g0052a0001c0005t0002g0188a0001c0005t0002g0195others(24): Show | 40 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1141-2108G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245352 | ||||||
chr15:50245357
|
AATGTTTA others(26): Show |
A | 1 | a0001c0001t0001g0028 | 3 | NA18957.hp2 NA18982.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1141-2146_1141-211 others(37): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245357 | ||||||
chr15:50245415
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1141-2171C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245415 | ||||||
chr15:50245646
|
G | A | 2 | a0001c0001t0003g0117a0001c0001t0003g0162 | 2 | HG01496.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1141-2402C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245646 | ||||||
chr15:50245691
|
G | T | 39 | a0001c0001t0001g0175a0001c0004t0001g0053a0001c0004t0001g0080others(36): Show | 53 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1141-2447C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245691 | ||||||
chr15:50245765
|
T | G | 1 | a0004c0006t0002g0190 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1140+2480A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245765 | ||||||
chr15:50245768
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(7): Show | 18 | HG00642.hp1 HG01081.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1140+2477C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245768 | ||||||
chr15:50245904
|
C | CAATA | 41 | a0001c0001t0001g0175a0001c0004t0001g0053a0001c0004t0001g0080others(38): Show | 58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1140+2337_1140+234 others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245904 | ||||||
chr15:50246127
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1140+2118C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246127 | ||||||
chr15:50246183
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1140+2062A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246183 | ||||||
chr15:50246189
|
C | T | 2 | a0003c0003t0001g0201a0003c0003t0001g0203 | 2 | HG00609.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1140+2056G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246189 | ||||||
chr15:50246252
|
C | T | 7 | a0001c0004t0001g0053a0001c0004t0001g0141a0001c0004t0001g0143others(4): Show | 8 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1140+1993G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246252 | ||||||
chr15:50246253
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1140+1992C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246253 | ||||||
chr15:50246478
|
T | G | 1 | a0001c0004t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1140+1767A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246478 | ||||||
chr15:50246533
|
C | T | 2 | a0002c0002t0002g0101a0002c0002t0002g0178 | 2 | HG02027.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1140+1712G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246533 | ||||||
chr15:50246655
|
G | T | 10 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(7): Show | 13 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1140+1590C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246655 | ||||||
chr15:50246872
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0129 | 2 | NA19000.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1140+1373C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246872 | ||||||
chr15:50246904
|
G | A | 3 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195 | 4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+1341C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246904 | ||||||
chr15:50246919
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1140+1326C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246919 | ||||||
chr15:50247023
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1140+1222G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247023 | ||||||
chr15:50247062
|
C | T | 1 | a0001c0001t0001g0044 | 2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1140+1183G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247062 | ||||||
chr15:50247195
|
T | C | 2 | a0001c0005t0002g0052a0001c0005t0002g0188 | 3 | HG01891.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1140+1050A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247195 | ||||||
chr15:50247199
|
C | T | 10 | a0001c0001t0001g0157a0001c0005t0002g0052a0001c0005t0002g0188others(7): Show | 14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1140+1046G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247199 | ||||||
chr15:50247271
|
A | G | 23 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(20): Show | 28 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1140+974T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247271 | ||||||
chr15:50247364
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0001g0115a0001c0001t0001g0159others(8): Show | 15 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1140+881G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247364 | ||||||
chr15:50247365
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1140+880C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247365 | ||||||
chr15:50247399
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1140+846A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247399 | ||||||
chr15:50247952
|
CTT | C | 29 | a0001c0001t0001g0115a0001c0001t0001g0152a0001c0004t0001g0053others(26): Show | 37 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+291_1140+292d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247952 | ||||||
chr15:50248145
|
G | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG01891.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+100C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50248145 | ||||||
chr15:50248504
|
G | A | 1 | a0001c0005t0001g0146 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1042-161C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248504 | ||||||
chr15:50248700
|
T | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1042-357A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248700 | ||||||
chr15:50248774
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1042-431T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248774 | ||||||
chr15:50248898
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1042-555G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248898 | ||||||
chr15:50249135
|
G | A | 1 | a0001c0001t0001g0037 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1042-792C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249135 | ||||||
chr15:50249396
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1042-1053G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249396 | ||||||
chr15:50249600
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1042-1257T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249600 | ||||||
chr15:50249663
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1042-1320T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249663 | ||||||
chr15:50249681
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0094a0001c0001t0001g0095 | 5 | HG01884.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1338T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249681 | ||||||
chr15:50249800
|
A | C | 1 | a0002c0002t0002g0023 | 3 | HG02451.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1042-1457T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249800 | ||||||
chr15:50249953
|
C | T | 3 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195 | 4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-1610G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249953 | ||||||
chr15:50249962
|
C | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(59): Show | 115 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1042-1619G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249962 | ||||||
chr15:50250056
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0118a0001c0001t0001g0137 | 3 | NA18959.hp2 NA18967.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1042-1713C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250056 | ||||||
chr15:50250173
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1042-1830T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250173 | ||||||
chr15:50250349
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1042-2006A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250349 | ||||||
chr15:50250419
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1041+2011C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250419 | ||||||
chr15:50250442
|
C | T | 1 | a0001c0005t0001g0146 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1041+1988G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250442 | ||||||
chr15:50250486
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1041+1944C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250486 | ||||||
chr15:50250522
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(51): Show | 104 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1041+1908T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250522 | ||||||
chr15:50250569
|
T | A | 1 | a0001c0001t0001g0028 | 3 | NA18957.hp2 NA18982.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1041+1861A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250569 | ||||||
chr15:50251056
|
C | T | 11 | a0001c0004t0001g0080a0001c0004t0001g0139a0001c0004t0001g0141others(8): Show | 12 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1041+1374G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251056 | ||||||
chr15:50251311
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1041+1119A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251311 | ||||||
chr15:50251326
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1041+1104C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251326 | ||||||
chr15:50251342
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG01891.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1041+1088C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251342 | ||||||
chr15:50251365
|
C | T | 1 | a0003c0003t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1041+1065G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251365 | ||||||
chr15:50251528
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1041+902G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251528 | ||||||
chr15:50251692
|
C | T | 1 | a0004c0006t0002g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1041+738G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251692 | ||||||
chr15:50251693
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1041+737C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251693 | ||||||
chr15:50251694
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0034others(21): Show | 45 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1041+736G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251694 | ||||||
chr15:50251704
|
C | G | 1 | a0001c0004t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1041+726G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251704 | ||||||
chr15:50251722
|
C | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0050others(4): Show | 10 | HG03942.hp2 NA18954.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+708G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251722 | ||||||
chr15:50251742
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1041+688C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251742 | ||||||
chr15:50251819
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1041+611C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251819 | ||||||
chr15:50251831
|
C | CA | 36 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0034others(33): Show | 61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1041+598dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251831 | ||||||
chr15:50251833
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1041+597C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251833 | ||||||
chr15:50251841
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1041+589T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251841 | ||||||
chr15:50251845
|
G | A | 2 | a0001c0005t0002g0052a0001c0005t0002g0188 | 3 | HG01891.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1041+585C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251845 | ||||||
chr15:50251874
|
AAG | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01167.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041+554_1041+555d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251874 | ||||||
chr15:50251933
|
T | C | 10 | a0001c0004t0001g0139a0001c0004t0001g0141a0001c0004t0001g0142others(7): Show | 11 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1041+497A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251933 | ||||||
chr15:50252012
|
C | CA | 12 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0189others(9): Show | 18 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1041+417dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252012 | ||||||
chr15:50252043
|
C | T | 6 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041+387G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252043 | ||||||
chr15:50252110
|
G | C | 2 | a0001c0005t0002g0052a0001c0005t0002g0188 | 3 | HG01891.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1041+320C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252110 | ||||||
chr15:50252348
|
C | T | 9 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195others(6): Show | 11 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1041+82G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252348 | ||||||
chr15:50252833
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0228 | 2 | HG01255.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.788-59C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252833 | ||||||
chr15:50252838
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0094 | 4 | HG01884.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-64A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252838 | ||||||
chr15:50252893
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.788-119C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252893 | ||||||
chr15:50252895
|
A | AG | 9 | a0001c0001t0001g0175a0002c0002t0002g0030a0002c0002t0002g0032others(6): Show | 13 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.788-122dupC | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252895 | ||||||
chr15:50252962
|
T | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(36): Show | 68 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.788-188A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252962 | ||||||
chr15:50252965
|
G | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(82): Show | 131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.788-191C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252965 | ||||||
chr15:50252973
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.788-199T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252973 | ||||||
chr15:50253049
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0026others(5): Show | 15 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.788-275G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253049 | ||||||
chr15:50253118
|
G | C | 1 | a0002c0008t0002g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.788-344C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253118 | ||||||
chr15:50253309
|
T | G | 2 | a0001c0005t0001g0013a0001c0005t0001g0057 | 5 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.787+291A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253309 | ||||||
chr15:50253358
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.787+242G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253358 | ||||||
chr15:50253569
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.787+31C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253569 | ||||||
chr15:50253773
|
A | G | 12 | a0001c0001t0001g0175a0001c0001t0001g0179a0002c0002t0002g0030others(9): Show | 18 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-107T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 6/11 | chr15 | 50253773 | ||||||
chr15:50254329
|
C | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.577-56G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 5/11 | chr15 | 50254329 | ||||||
chr15:50254353
|
C | T | 3 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195 | 4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-80G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 5/11 | chr15 | 50254353 | ||||||
chr15:50254733
|
GTT | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0056others(25): Show | 41 | HG00423.hp2 HG01891.hp2 HG02027.hp1 others(38): Show |
intron_variant | MODIFIER | c.442-71_442-70delAA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254733 | ||||||
chr15:50254736
|
T | TCTCTCTC others(4): Show |
1 | a0001c0004t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-73_442-72insGA others(9): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | ||||||
chr15:50254736
|
T | TTCTCTCT others(3): Show |
1 | a0001c0005t0001g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.442-73_442-72insGA others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | ||||||
chr15:50254736
|
TTTTC | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(34): Show | 82 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.442-76_442-73delGA others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | ||||||
chr15:50254736
|
TTTTCTC | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0153a0001c0001t0001g0168others(1): Show | 4 | HG01256.hp2 HG02165.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-78_442-73delGA others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | ||||||
chr15:50254738
|
T | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0045others(16): Show | 28 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-74A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
T | TTC | 8 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0040others(5): Show | 27 | HG00323.hp2 HG00597.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-76_442-75dupGA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
T | TTCTC | 4 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0089others(1): Show | 14 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-78_442-75dupGA others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
T | TTCTCTC | 4 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(1): Show | 5 | HG01168.hp2 HG01169.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-80_442-75dupGA others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
T | TTCTCTCT others(1): Show |
4 | a0001c0004t0001g0053a0002c0007t0001g0060a0002c0007t0001g0061others(1): Show | 5 | HG00099.hp1 HG01074.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-82_442-75dupGA others(6): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
T | TTCTCTCT others(3): Show |
3 | a0001c0004t0001g0196a0001c0005t0002g0195a0002c0007t0001g0036 | 4 | HG01099.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-84_442-75dupGA others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
T | TTCTCTCT others(5): Show |
1 | a0002c0007t0001g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.442-86_442-75dupGA others(10): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
TTC | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0064others(11): Show | 19 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-76_442-75delGA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
TTCTC | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0073others(10): Show | 20 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.442-78_442-75delGA others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
TTCTCTC | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(32): Show | 63 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-80_442-75delGA others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
TTCTCTCT others(1): Show |
T | 12 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0094others(9): Show | 19 | HG00323.hp1 HG00639.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.442-82_442-75delGA others(6): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254738
|
TTCTCTCT others(11): Show |
T | 3 | a0004c0006t0002g0021a0004c0006t0002g0145a0004c0006t0002g0233 | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-92_442-75delGA others(16): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | ||||||
chr15:50254740
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.442-76G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254740 | ||||||
chr15:50254744
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-80G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254744 | ||||||
chr15:50254772
|
C | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0175a0001c0001t0001g0192others(3): Show | 6 | HG03041.hp1 HG03471.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-108G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254772 | ||||||
chr15:50254774
|
C | G | 57 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(54): Show | 95 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.442-110G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254774 | ||||||
chr15:50254776
|
C | CTCTCTCT others(1): Show |
3 | a0001c0004t0001g0142a0001c0004t0001g0143a0002c0007t0001g0059 | 3 | HG00733.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.442-113_442-112ins others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254776 | ||||||
chr15:50254776
|
C | CTG | 3 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0067 | 6 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-114_442-113dup others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254776 | ||||||
chr15:50254776
|
C | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(58): Show | 99 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.442-112G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254776 | ||||||
chr15:50254778
|
G | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18966.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.442-114C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254778 | ||||||
chr15:50254987
|
C | T | 1 | a0003c0003t0001g0205 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.442-323G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254987 | ||||||
chr15:50255209
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.442-545C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255209 | ||||||
chr15:50255673
|
A | G | 1 | a0003c0003t0001g0185 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.442-1009T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255673 | ||||||
chr15:50255690
|
C | T | 1 | a0001c0004t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-1026G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255690 | ||||||
chr15:50255691
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 7 | HG01123.hp1 HG01257.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1027C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255691 | ||||||
chr15:50255787
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.442-1123G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255787 | ||||||
chr15:50255857
|
A | G | 9 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195others(6): Show | 11 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-1193T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255857 | ||||||
chr15:50255971
|
A | G | 8 | a0001c0001t0001g0181a0001c0001t0001g0207a0001c0004t0001g0139others(5): Show | 11 | HG01109.hp2 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-1307T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255971 | ||||||
chr15:50256046
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(40): Show | 91 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.441+1379G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256046 | ||||||
chr15:50256058
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.441+1367C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256058 | ||||||
chr15:50256058
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0094 | 4 | HG01884.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+1367C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256058 | ||||||
chr15:50256121
|
G | C | 3 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195 | 4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1304C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256121 | ||||||
chr15:50256230
|
C | T | 1 | a0001c0001t0001g0037 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.441+1195G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256230 | ||||||
chr15:50256366
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0189others(7): Show | 15 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+1059C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256366 | ||||||
chr15:50256470
|
C | T | 1 | a0001c0004t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.441+955G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256470 | ||||||
chr15:50256630
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.441+795A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256630 | ||||||
chr15:50256688
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.441+737C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256688 | ||||||
chr15:50256759
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+666A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256759 | ||||||
chr15:50256865
|
T | C | 3 | a0004c0006t0002g0021a0004c0006t0002g0145a0004c0006t0002g0233 | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+560A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256865 | ||||||
chr15:50256899
|
A | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG01109.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.441+526T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256899 | ||||||
chr15:50257007
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.441+418C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257007 | ||||||
chr15:50257380
|
G | A | 1 | a0002c0008t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+45C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257380 | ||||||
chr15:50257391
|
C | G | 4 | a0002c0008t0002g0230a0004c0006t0002g0021a0004c0006t0002g0145others(1): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+34G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257391 | ||||||
chr15:50257395
|
A | T | 4 | a0002c0008t0002g0230a0004c0006t0002g0021a0004c0006t0002g0145others(1): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+30T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257395 | ||||||
chr15:50257827
|
C | T | 1 | a0002c0008t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.319-280G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50257827 | ||||||
chr15:50257870
|
T | A | 1 | a0002c0008t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.319-323A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50257870 | ||||||
chr15:50258041
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.318+363G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258041 | ||||||
chr15:50258200
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.318+204T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258200 | ||||||
chr15:50258364
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318+40T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258364 | ||||||
chr15:50258378
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG02074.hp2 NA18977.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.318+26C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258378 | ||||||
chr15:50258544
|
G | T | 5 | a0001c0004t0001g0139a0001c0004t0001g0141a0001c0004t0001g0142others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-27C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258544 | ||||||
chr15:50258703
|
C | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(36): Show | 68 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.205-186G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258703 | ||||||
chr15:50258785
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.205-268G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258785 | ||||||
chr15:50258813
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.205-296C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258813 | ||||||
chr15:50258886
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 251 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.205-369A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258886 | ||||||
chr15:50258906
|
A | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(81): Show | 151 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.205-389T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258906 | ||||||
chr15:50258988
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(105): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.205-471T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258988 | ||||||
chr15:50259005
|
C | CA | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(103): Show | 178 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.205-489dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259005 | ||||||
chr15:50259005
|
C | CAA | 2 | a0004c0006t0002g0021a0004c0006t0002g0233 | 5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-490_205-489dup others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259005 | ||||||
chr15:50259140
|
C | T | 1 | a0001c0012t0001g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205-623G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259140 | ||||||
chr15:50259163
|
A | G | 36 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(33): Show | 50 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.205-646T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259163 | ||||||
chr15:50259389
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.205-872A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259389 | ||||||
chr15:50259398
|
G | A | 12 | a0001c0001t0001g0207a0003c0003t0001g0020a0003c0003t0001g0185others(9): Show | 15 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.205-881C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259398 | ||||||
chr15:50259435
|
G | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(68): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.205-918C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259435 | ||||||
chr15:50259444
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.205-927C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259444 | ||||||
chr15:50259507
|
G | A | 12 | a0003c0003t0001g0019a0003c0003t0001g0020a0003c0003t0001g0185others(9): Show | 18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-990C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259507 | ||||||
chr15:50259577
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.205-1060T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259577 | ||||||
chr15:50259658
|
G | T | 12 | a0003c0003t0001g0019a0003c0003t0001g0020a0003c0003t0001g0185others(9): Show | 18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-1141C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259658 | ||||||
chr15:50259722
|
C | T | 2 | a0004c0006t0002g0021a0004c0006t0002g0233 | 5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-1205G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259722 | ||||||
chr15:50259733
|
C | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(36): Show | 68 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.205-1216G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259733 | ||||||
chr15:50260023
|
CT | C | 10 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0189others(7): Show | 15 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-1507delA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260023 | ||||||
chr15:50260023
|
CTT | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 187 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-1508_205-1507d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260023 | ||||||
chr15:50260105
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.205-1588G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260105 | ||||||
chr15:50260153
|
C | T | 1 | a0001c0004t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.205-1636G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260153 | ||||||
chr15:50260172
|
C | G | 1 | a0001c0004t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.205-1655G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260172 | ||||||
chr15:50260175
|
C | T | 1 | a0002c0008t0002g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.205-1658G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260175 | ||||||
chr15:50260256
|
C | A | 2 | a0001c0001t0001g0207a0002c0008t0002g0230 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.205-1739G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260256 | ||||||
chr15:50260301
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.205-1784T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260301 | ||||||
chr15:50260388
|
G | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(36): Show | 68 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.205-1871C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260388 | ||||||
chr15:50260554
|
A | T | 1 | a0001c0004t0001g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.205-2037T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260554 | ||||||
chr15:50260658
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 138 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.205-2141G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260658 | ||||||
chr15:50260803
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(47): Show | 85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.205-2286C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260803 | ||||||
chr15:50260830
|
G | T | 1 | a0001c0001t0001g0037 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.205-2313C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260830 | ||||||
chr15:50260880
|
A | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0033others(47): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.204+2355T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260880 | ||||||
chr15:50261176
|
T | G | 1 | a0002c0002t0002g0032 | 3 | NA18980.hp2 NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.204+2059A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261176 | ||||||
chr15:50261226
|
G | A | 1 | a0002c0002t0002g0032 | 3 | NA18980.hp2 NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.204+2009C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261226 | ||||||
chr15:50261227
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.204+2008G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261227 | ||||||
chr15:50261307
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.204+1928A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261307 | ||||||
chr15:50261574
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.204+1661T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261574 | ||||||
chr15:50261623
|
C | CA | 86 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.204+1611dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261623 | ||||||
chr15:50261623
|
C | CAA | 16 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0128others(13): Show | 19 | HG00280.hp1 HG00597.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+1610_204+1611d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261623 | ||||||
chr15:50261623
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0022a0001c0001t0001g0067 | 4 | HG01243.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+1602_204+1611d others(12): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261623 | ||||||
chr15:50261675
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1560A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261675 | ||||||
chr15:50261678
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1557A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261678 | ||||||
chr15:50261682
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1553G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261682 | ||||||
chr15:50261683
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1552G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261683 | ||||||
chr15:50261686
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1549G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261686 | ||||||
chr15:50261688
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1547G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261688 | ||||||
chr15:50261691
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1544G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261691 | ||||||
chr15:50261703
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1532A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261703 | ||||||
chr15:50261709
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1526A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261709 | ||||||
chr15:50261711
|
A | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1524T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261711 | ||||||
chr15:50261712
|
C | CTT | 8 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195others(5): Show | 10 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+1521_204+1522d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261712 | ||||||
chr15:50261712
|
CT | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(48): Show | 86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.204+1522delA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261712 | ||||||
chr15:50261721
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1514A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261721 | ||||||
chr15:50261740
|
G | A | 1 | a0002c0008t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+1495C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261740 | ||||||
chr15:50261743
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1492G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261743 | ||||||
chr15:50261747
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1488A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261747 | ||||||
chr15:50261748
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1487A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261748 | ||||||
chr15:50261754
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1481C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261754 | ||||||
chr15:50261755
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1480C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261755 | ||||||
chr15:50261756
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1479G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261756 | ||||||
chr15:50261757
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1478A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261757 | ||||||
chr15:50261760
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.204+1475T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261760 | ||||||
chr15:50261763
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1472C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261763 | ||||||
chr15:50261769
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1466C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261769 | ||||||
chr15:50261776
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1459G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261776 | ||||||
chr15:50261779
|
A | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1456T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261779 | ||||||
chr15:50261790
|
A | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1445T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261790 | ||||||
chr15:50261796
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1439C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261796 | ||||||
chr15:50261803
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(38): Show | 73 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.204+1432C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261803 | ||||||
chr15:50261805
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.204+1430C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261805 | ||||||
chr15:50261806
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1429A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261806 | ||||||
chr15:50261829
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1406G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261829 | ||||||
chr15:50261831
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1404A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261831 | ||||||
chr15:50261832
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1403G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261832 | ||||||
chr15:50261833
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1402G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261833 | ||||||
chr15:50261835
|
A | G | 5 | a0001c0004t0001g0139a0001c0004t0001g0141a0001c0004t0001g0142others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1400T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261835 | ||||||
chr15:50261898
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.204+1337C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261898 | ||||||
chr15:50262075
|
A | C | 2 | a0004c0006t0002g0021a0004c0006t0002g0233 | 5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1160T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262075 | ||||||
chr15:50262113
|
C | T | 1 | a0002c0008t0002g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.204+1122G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262113 | ||||||
chr15:50262198
|
A | T | 1 | a0001c0004t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.204+1037T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262198 | ||||||
chr15:50262301
|
T | C | 2 | a0001c0001t0001g0207a0004c0006t0002g0190 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.204+934A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262301 | ||||||
chr15:50262332
|
C | G | 1 | a0003c0003t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.204+903G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262332 | ||||||
chr15:50262336
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.204+899C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262336 | ||||||
chr15:50262426
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0155 | 3 | HG01081.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.204+809C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262426 | ||||||
chr15:50262496
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0050others(16): Show | 36 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.204+739C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262496 | ||||||
chr15:50262814
|
C | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(87): Show | 151 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.204+421G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262814 | ||||||
chr15:50262904
|
A | G | 1 | a0001c0010t0001g0138 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.204+331T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262904 | ||||||
chr15:50262930
|
TC | T | 8 | a0001c0001t0001g0065a0003c0003t0001g0020a0003c0003t0001g0199others(5): Show | 11 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+304delG | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262930 | ||||||
chr15:50262964
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.204+271G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262964 | ||||||
chr15:50263039
|
A | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0033others(31): Show | 58 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.204+196T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50263039 | ||||||
chr15:50263484
|
C | T | 1 | a0002c0007t0001g0059 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.32-77G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263484 | ||||||
chr15:50263513
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(125): Show | 205 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.32-106A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263513 | ||||||
chr15:50263583
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.32-176G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263583 | ||||||
chr15:50263661
|
G | T | 5 | a0002c0007t0001g0036a0002c0007t0001g0059a0002c0007t0001g0060others(2): Show | 6 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-254C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263661 | ||||||
chr15:50263667
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0033others(34): Show | 64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.32-260C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263667 | ||||||
chr15:50263758
|
C | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG01891.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-351G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263758 | ||||||
chr15:50263776
|
G | C | 3 | a0001c0004t0001g0053a0001c0004t0001g0196a0001c0005t0002g0195 | 4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-369C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263776 | ||||||
chr15:50263776
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.32-369C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263776 | ||||||
chr15:50263948
|
G | A | 1 | a0002c0008t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.32-541C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263948 | ||||||
chr15:50264229
|
G | A | 2 | a0004c0006t0002g0021a0004c0006t0002g0233 | 5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-822C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264229 | ||||||
chr15:50264395
|
G | A | 1 | a0002c0002t0002g0197 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.32-988C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264395 | ||||||
chr15:50264424
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0206a0001c0001t0001g0231 | 5 | HG00544.hp2 NA18942.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-1017T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264424 | ||||||
chr15:50264769
|
C | A | 1 | a0001c0001t0001g0231 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.31+824G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264769 | ||||||
chr15:50264800
|
C | G | 13 | a0002c0007t0001g0036a0002c0007t0001g0059a0002c0007t0001g0060others(10): Show | 17 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.31+793G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264800 | ||||||
chr15:50264879
|
G | C | 1 | a0001c0004t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31+714C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264879 | ||||||
chr15:50264915
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31+678T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264915 | ||||||
chr15:50264962
|
G | A | 8 | a0003c0003t0001g0020a0003c0003t0001g0199a0003c0003t0001g0200others(5): Show | 11 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.31+631C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264962 | ||||||
chr15:50265134
|
T | G | 1 | a0002c0007t0001g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31+459A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265134 | ||||||
chr15:50265185
|
A | T | 2 | a0004c0006t0002g0021a0004c0006t0002g0233 | 5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+408T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265185 | ||||||
chr15:50265255
|
C | A | 1 | a0004c0006t0002g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+338G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265255 | ||||||
chr15:50265403
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 4 | HG01496.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+190C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265403 | ||||||
chr15:50265532
|
C | G | 2 | a0001c0005t0001g0013a0001c0005t0001g0057 | 5 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+61G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265532 | ||||||
chr15:50265541
|
G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0033others(32): Show | 61 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.31+52C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265541 |