geneid | 51166 |
---|---|
ensemblid | ENSG00000109576.14 |
hgncid | 17929 |
symbol | AADAT |
name | aminoadipate aminotransferase |
refseq_nuc | NM_016228.4 |
refseq_prot | NP_057312.1 |
ensembl_nuc | ENST00000337664.9 |
ensembl_prot | ENSP00000336808.4 |
mane_status | MANE Select |
chr | chr4 |
start | 170060222 |
end | 170089956 |
strand | - |
ver | v1.2 |
region | chr4:170060222-170089956 |
region5000 | chr4:170055222-170094956 |
regionname0 | AADAT_chr4_170060222_170089956 |
regionname5000 | AADAT_chr4_170055222_170094956 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 425 | 378 | 94 | 62 | 154 | 18 | 48 | 122 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1278 | 365 | 94 | 62 | 141 | 18 | 48 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
c0002 | 0/0 | 1278 | 13 | 0 | 0 | 13 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 973 | 349 | 88 | 54 | 149 | 17 | 40 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0002 | 0/1 | 973 | 13 | 3 | 3 | 2 | 1 | 3 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0003 | 0/0 | 972 | 10 | 0 | 4 | 1 | 0 | 5 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0004 | 0/0 | 973 | 2 | 1 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0005 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0006 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0007 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
t0008 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 24 | 0 | 4 | 15 | 1 | 4 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0002 | 0/0 | 23 | 3 | 9 | 2 | 3 | 6 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0003 | 0/0 | 21 | 0 | 0 | 16 | 0 | 5 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0004 | 0/0 | 15 | 0 | 1 | 12 | 1 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0005 | 0/0 | 13 | 1 | 0 | 12 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0008 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0010 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0014 | 0/0 | 5 | 0 | 1 | 0 | 4 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0019 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0029 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1278 | 365 | 94 | 62 | 141 | 18 | 48 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0002 | 0/0 | 1278 | 13 | 0 | 0 | 13 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2250 | 336 | 88 | 54 | 136 | 17 | 40 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0002 | 0/1 | 2250 | 13 | 3 | 3 | 2 | 1 | 3 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0003 | 0/0 | 2249 | 10 | 0 | 4 | 1 | 0 | 5 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0004 | 0/0 | 2250 | 2 | 1 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0005 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0006 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0007 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0001t0008 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
a0001c0002t0001 | 0/0 | 2250 | 13 | 0 | 0 | 13 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | copy fasta | chr4 | 170055222 | 170094956 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 24 | 0 | 4 | 15 | 1 | 4 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0002 | 0/0 | 23 | 3 | 9 | 2 | 3 | 6 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0003 | 0/0 | 21 | 0 | 0 | 16 | 0 | 5 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0004 | 0/0 | 15 | 0 | 1 | 12 | 1 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0005 | 0/0 | 13 | 1 | 0 | 12 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 0 | 4 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0019 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0029 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0010 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0004g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | CHB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18948 | hp2 | a0001 | c0001 | t0008 | g0159 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | GIH | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0058 | REF | REF | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0029 | REF | REF | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:170073199
|
A | G | 1 | a0001c0002 | 13 | HG00438.hp2 HG00609.hp1 NA18941.hp1 others(10): Show |
synonymous_variant | LOW | c.591T>C | p.Val197Val | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/13 | 857/2250 | 591/1278 | 197/425 | chr4 | 170073199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:170060238
|
A | T | 1 | a0001c0001t0007 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 690 | chr4 | 170060238 | |||||
chr4:170060288
|
T | A | 1 | a0001c0001t0008 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 640 | chr4 | 170060288 | |||||
chr4:170060293
|
A | G | 1 | a0001c0001t0006 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 635 | chr4 | 170060293 | |||||
chr4:170060317
|
TA | T | 1 | a0001c0001t0003 | 10 | HG01109.hp2 HG01123.hp1 HG01168.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*610delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 610 | chr4 | 170060317 | |||||
chr4:170060442
|
T | C | 1 | a0001c0001t0008 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 486 | chr4 | 170060442 | |||||
chr4:170060632
|
G | T | 1 | a0001c0001t0002 | 13 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*296C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 296 | chr4 | 170060632 | |||||
chr4:170060796
|
C | A | 1 | a0001c0001t0004 | 2 | HG00639.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*132G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 132 | chr4 | 170060796 | |||||
chr4:170089905
|
G | T | 1 | a0001c0001t0005 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-215C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/13 | 215 | chr4 | 170089905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:170060989
|
T | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0186 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1237-20A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170060989 | ||||||
chr4:170061166
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1237-197C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061166 | ||||||
chr4:170061443
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1236+449A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061443 | ||||||
chr4:170061535
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1236+357G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061535 | ||||||
chr4:170061639
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0076others(6): Show | 12 | HG02451.hp2 HG02559.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1236+253G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061639 | ||||||
chr4:170062318
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1135-325A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062318 | ||||||
chr4:170062561
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1135-568G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062561 | ||||||
chr4:170062676
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0205 | 2 | HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1135-683G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062676 | ||||||
chr4:170062692
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1135-699C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062692 | ||||||
chr4:170062709
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1135-716C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062709 | ||||||
chr4:170062736
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1135-743A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062736 | ||||||
chr4:170062771
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1135-778A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062771 | ||||||
chr4:170062965
|
C | CT | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1135-973dupA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062965 | ||||||
chr4:170063078
|
T | C | 1 | a0001c0001t0001g0040 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1135-1085A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063078 | ||||||
chr4:170063254
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135-1261G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063254 | ||||||
chr4:170063509
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1134+1210A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063509 | ||||||
chr4:170063598
|
T | C | 2 | a0001c0001t0002g0053a0001c0001t0002g0057 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1134+1121A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063598 | ||||||
chr4:170063603
|
T | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0138others(4): Show | 10 | HG02559.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+1116A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063603 | ||||||
chr4:170063631
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1134+1088T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063631 | ||||||
chr4:170063674
|
C | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1134+1045G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063674 | ||||||
chr4:170063707
|
C | T | 1 | a0001c0001t0001g0038 | 2 | NA18942.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1134+1012G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063707 | ||||||
chr4:170063803
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1134+916T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063803 | ||||||
chr4:170063871
|
G | A | 1 | a0001c0001t0004g0047 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+848C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063871 | ||||||
chr4:170063956
|
AG | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1134+762delC | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063956 | ||||||
chr4:170063958
|
GA | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0020others(11): Show | 31 | HG00423.hp2 HG00621.hp1 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.1134+760delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063958 | ||||||
chr4:170063967
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+752T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063967 | ||||||
chr4:170064036
|
A | G | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1134+683T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064036 | ||||||
chr4:170064167
|
C | G | 1 | a0001c0001t0001g0043 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1134+552G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064167 | ||||||
chr4:170064193
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1134+526G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064193 | ||||||
chr4:170064196
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1134+523G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064196 | ||||||
chr4:170064247
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1134+472A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064247 | ||||||
chr4:170064258
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1134+461T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064258 | ||||||
chr4:170064361
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1134+358G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064361 | ||||||
chr4:170064436
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1134+283A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064436 | ||||||
chr4:170064479
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1134+240A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064479 | ||||||
chr4:170064688
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+31C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064688 | ||||||
chr4:170064689
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1134+30C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064689 | ||||||
chr4:170064704
|
A | ACCT | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1134+12_1134+14dup others(3): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064704 | ||||||
chr4:170064834
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1028-9T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170064834 | ||||||
chr4:170065060
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1028-235C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065060 | ||||||
chr4:170065129
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028-304A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065129 | ||||||
chr4:170065154
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0076 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1028-329C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065154 | ||||||
chr4:170065157
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1028-332T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065157 | ||||||
chr4:170065222
|
C | G | 1 | a0001c0001t0001g0007 | 6 | HG01109.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028-397G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065222 | ||||||
chr4:170065428
|
T | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028-603A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065428 | ||||||
chr4:170065509
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1028-684C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065509 | ||||||
chr4:170065646
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1027+768C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065646 | ||||||
chr4:170065654
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1027+760A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065654 | ||||||
chr4:170066045
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027+369T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170066045 | ||||||
chr4:170066120
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1027+294A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170066120 | ||||||
chr4:170066203
|
C | A | 14 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0016others(11): Show | 17 | HG00323.hp1 HG00639.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1027+211G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170066203 | ||||||
chr4:170066485
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 324 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(321): Show |
splice_region_variant&intron_variant | LOW | c.963-7T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066485 | ||||||
chr4:170066764
|
GTTGTCTA others(5): Show |
G | 2 | a0001c0001t0001g0044a0001c0001t0001g0189 | 3 | HG02622.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.963-298_963-287del others(12): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066764 | ||||||
chr4:170066887
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.963-409A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066887 | ||||||
chr4:170066948
|
T | A | 1 | a0001c0001t0003g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.962+379A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066948 | ||||||
chr4:170066952
|
C | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0053a0001c0001t0002g0054others(8): Show | 13 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.962+375G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066952 | ||||||
chr4:170066980
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.962+347G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066980 | ||||||
chr4:170066981
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0097 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.962+346C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066981 | ||||||
chr4:170067069
|
C | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG03130.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.962+258G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067069 | ||||||
chr4:170067153
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.962+174A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067153 | ||||||
chr4:170067200
|
C | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0026others(22): Show | 37 | HG00733.hp2 HG01257.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.962+127G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067200 | ||||||
chr4:170067319
|
T | G | 1 | a0001c0001t0004g0047 | 2 | HG00639.hp2 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.962+8A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067319 | ||||||
chr4:170067748
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.901-360G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067748 | ||||||
chr4:170067804
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901-416A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067804 | ||||||
chr4:170067908
|
A | G | 1 | a0001c0001t0001g0040 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.901-520T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067908 | ||||||
chr4:170067995
|
C | T | 1 | a0001c0001t0001g0011 | 5 | HG00558.hp1 NA18950.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+596G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067995 | ||||||
chr4:170068064
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.900+527C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068064 | ||||||
chr4:170068068
|
T | C | 1 | a0001c0001t0003g0070 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.900+523A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068068 | ||||||
chr4:170068138
|
C | CA | 21 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0123others(18): Show | 29 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.900+452dupT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068138 | ||||||
chr4:170068138
|
CA | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0017others(36): Show | 74 | HG00408.hp2 HG00609.hp2 HG01168.hp2 others(71): Show |
intron_variant | MODIFIER | c.900+452delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068138 | ||||||
chr4:170068138
|
CAA | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0072a0001c0001t0001g0075others(2): Show | 6 | HG02258.hp2 HG02922.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+451_900+452del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068138 | ||||||
chr4:170068557
|
C | CA | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 275 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.900+33dupT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068557 | ||||||
chr4:170068557
|
C | CAA | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.900+32_900+33dupTT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068557 | ||||||
chr4:170068710
|
C | T | 1 | a0001c0001t0004g0047 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.804-23G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068710 | ||||||
chr4:170068831
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.804-144A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068831 | ||||||
chr4:170068878
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.804-191A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068878 | ||||||
chr4:170068902
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 150 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.804-215G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068902 | ||||||
chr4:170069296
|
G | T | 1 | a0001c0001t0004g0047 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721-66C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069296 | ||||||
chr4:170069494
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-264T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069494 | ||||||
chr4:170069520
|
C | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0053a0001c0001t0002g0054others(8): Show | 13 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-290G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069520 | ||||||
chr4:170069564
|
T | A | 1 | a0001c0001t0001g0035 | 2 | HG02683.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.721-334A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069564 | ||||||
chr4:170069599
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-369C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069599 | ||||||
chr4:170069625
|
C | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 8 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-395G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069625 | ||||||
chr4:170069732
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.721-502T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069732 | ||||||
chr4:170069795
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.721-565A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069795 | ||||||
chr4:170069860
|
C | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-630G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069860 | ||||||
chr4:170069879
|
C | A | 1 | a0001c0001t0001g0202 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721-649G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069879 | ||||||
chr4:170069905
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0186 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.721-675A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069905 | ||||||
chr4:170070105
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.720+482G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070105 | ||||||
chr4:170070111
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.720+476A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070111 | ||||||
chr4:170070334
|
T | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0138others(4): Show | 10 | HG02559.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+253A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070334 | ||||||
chr4:170070367
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.720+220A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070367 | ||||||
chr4:170070442
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.720+145A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070442 | ||||||
chr4:170070487
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.720+100C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070487 | ||||||
chr4:170070494
|
TCTGACTC others(16): Show |
T | 1 | a0001c0001t0002g0055 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.720+70_720+92delTA others(21): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070494 | ||||||
chr4:170070660
|
AGGTT | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 150 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.655-12_655-9delAAC others(1): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170070660 | ||||||
chr4:170070787
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0200a0001c0001t0001g0201 | 7 | HG00099.hp2 HG01070.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-135G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170070787 | ||||||
chr4:170071215
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.655-563T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071215 | ||||||
chr4:170071396
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.655-744A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071396 | ||||||
chr4:170071523
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0200others(2): Show | 10 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.655-871G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071523 | ||||||
chr4:170071553
|
G | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0200others(2): Show | 10 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.655-901C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071553 | ||||||
chr4:170071609
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0200others(2): Show | 10 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.655-957C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071609 | ||||||
chr4:170071615
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.655-963C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071615 | ||||||
chr4:170071702
|
G | A | 10 | a0001c0001t0002g0016a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 12 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.655-1050C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071702 | ||||||
chr4:170071962
|
A | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0100 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.654+1174T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071962 | ||||||
chr4:170072025
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.654+1111C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072025 | ||||||
chr4:170072137
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.654+999C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072137 | ||||||
chr4:170072211
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0166 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.654+911_654+924del others(14): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072211 | ||||||
chr4:170072241
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(24): Show | 54 | HG00408.hp2 HG00609.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.654+895C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072241 | ||||||
chr4:170072253
|
AGATAC | A | 28 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(25): Show | 55 | HG00408.hp2 HG00609.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.654+878_654+882del others(5): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072253 | ||||||
chr4:170072261
|
GTA | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+873_654+874del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072261 | ||||||
chr4:170072299
|
G | GTA | 60 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(57): Show | 100 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+835_654+836dup others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072299 | ||||||
chr4:170072299
|
G | GTATA | 5 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0087others(2): Show | 10 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+833_654+836dup others(4): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072299 | ||||||
chr4:170072299
|
GTA | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0111others(2): Show | 7 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+835_654+836del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072299 | ||||||
chr4:170072301
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+835T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072301 | ||||||
chr4:170072312
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0188a0001c0001t0001g0190 | 4 | HG01358.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+824A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072312 | ||||||
chr4:170072398
|
G | C | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.654+738C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072398 | ||||||
chr4:170072429
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0076 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.654+707G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072429 | ||||||
chr4:170072525
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0132 | 3 | HG00438.hp1 NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.654+611A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072525 | ||||||
chr4:170072579
|
T | C | 10 | a0001c0001t0002g0016a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 12 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+557A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072579 | ||||||
chr4:170072620
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 302 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.654+516T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072620 | ||||||
chr4:170072659
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 8 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+477A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072659 | ||||||
chr4:170072832
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.654+304A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072832 | ||||||
chr4:170072843
|
C | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0041 | 7 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+293G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072843 | ||||||
chr4:170073054
|
G | C | 14 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 17 | HG01358.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.654+82C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170073054 | ||||||
chr4:170073390
|
G | A | 1 | a0001c0001t0001g0021 | 3 | HG03041.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445-45C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073390 | ||||||
chr4:170073403
|
GT | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 301 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.445-59delA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073403 | ||||||
chr4:170073510
|
TA | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0192a0001c0001t0008g0159 | 3 | HG01975.hp2 HG02145.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.445-166delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073510 | ||||||
chr4:170073511
|
A | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 302 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.445-166T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073511 | ||||||
chr4:170073515
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-170A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073515 | ||||||
chr4:170073545
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-200G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073545 | ||||||
chr4:170073617
|
G | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0195 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-272C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073617 | ||||||
chr4:170073630
|
C | T | 1 | a0001c0001t0001g0039 | 2 | NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.445-285G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073630 | ||||||
chr4:170073663
|
G | C | 1 | a0001c0001t0001g0021 | 3 | HG03041.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445-318C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073663 | ||||||
chr4:170073687
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.445-342C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073687 | ||||||
chr4:170073701
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0072 | 3 | NA19004.hp1 NA19007.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.445-356T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073701 | ||||||
chr4:170073723
|
T | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0186 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.445-378A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073723 | ||||||
chr4:170073743
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 9 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-398G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073743 | ||||||
chr4:170073767
|
A | G | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0119others(2): Show | 5 | HG00140.hp2 HG01243.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-422T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073767 | ||||||
chr4:170073785
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0129 | 3 | HG01168.hp1 HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445-440A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073785 | ||||||
chr4:170073786
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0129 | 3 | HG01168.hp1 HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445-441C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073786 | ||||||
chr4:170073899
|
CAGTGGGC others(15): Show |
C | 3 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0195 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-576_445-555del others(22): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073899 | ||||||
chr4:170073915
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(33): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.445-570G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073915 | ||||||
chr4:170073933
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0130 | 3 | HG02683.hp1 HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.445-588A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073933 | ||||||
chr4:170074018
|
G | T | 5 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0142others(2): Show | 13 | HG00438.hp2 HG00609.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-673C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074018 | ||||||
chr4:170074026
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.445-681A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074026 | ||||||
chr4:170074085
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.445-740A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074085 | ||||||
chr4:170074162
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 9 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-817G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074162 | ||||||
chr4:170074294
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 101 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.445-949G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074294 | ||||||
chr4:170074328
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(53): Show | 99 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.445-983A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074328 | ||||||
chr4:170074347
|
T | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0188others(2): Show | 7 | HG01358.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-1002A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074347 | ||||||
chr4:170074470
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.445-1125G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074470 | ||||||
chr4:170074505
|
CAT | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-1162_445-1161d others(4): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074505 | ||||||
chr4:170074534
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0067 | 3 | HG00733.hp2 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.445-1189A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074534 | ||||||
chr4:170074718
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 8 | HG00099.hp2 HG01070.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-1373G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074718 | ||||||
chr4:170074740
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0195 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1395T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074740 | ||||||
chr4:170074748
|
AG | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0096 | 3 | HG02886.hp2 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.445-1404delC | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074748 | ||||||
chr4:170074800
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0195 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1455A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074800 | ||||||
chr4:170074857
|
G | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0188others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-1512C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074857 | ||||||
chr4:170074957
|
A | C | 1 | a0001c0001t0002g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.445-1612T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074957 | ||||||
chr4:170075148
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.445-1803A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075148 | ||||||
chr4:170075165
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0002g0137a0001c0001t0002g0204 | 3 | HG02451.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.445-1820C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075165 | ||||||
chr4:170075179
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(50): Show | 95 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.445-1834C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075179 | ||||||
chr4:170075264
|
C | T | 8 | a0001c0001t0002g0016a0001c0001t0002g0053a0001c0001t0002g0054others(5): Show | 10 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.445-1919G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075264 | ||||||
chr4:170075407
|
T | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-2062A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075407 | ||||||
chr4:170075605
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445-2260T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075605 | ||||||
chr4:170075632
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0076 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.445-2287G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075632 | ||||||
chr4:170075923
|
T | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0058 | 4 | HG01255.hp2 HG01433.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-2578A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075923 | ||||||
chr4:170075928
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.444+2581G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075928 | ||||||
chr4:170076063
|
G | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+2446C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076063 | ||||||
chr4:170076335
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.444+2174A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076335 | ||||||
chr4:170076362
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.444+2147A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076362 | ||||||
chr4:170076426
|
C | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0194others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+2083G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076426 | ||||||
chr4:170076506
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+2003G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076506 | ||||||
chr4:170076772
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+1737T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076772 | ||||||
chr4:170076821
|
TC | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+1687delG | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076821 | ||||||
chr4:170076832
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.444+1677A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076832 | ||||||
chr4:170076872
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+1637C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076872 | ||||||
chr4:170076906
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0188 | 3 | HG02258.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.444+1603G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076906 | ||||||
chr4:170077034
|
A | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG02055.hp1 HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.444+1475T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077034 | ||||||
chr4:170077411
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.444+1098A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077411 | ||||||
chr4:170077430
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0195others(2): Show | 9 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+1079G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077430 | ||||||
chr4:170077539
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.444+970A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077539 | ||||||
chr4:170077577
|
G | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+932C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077577 | ||||||
chr4:170077748
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0076 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.444+761T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077748 | ||||||
chr4:170077915
|
C | G | 1 | a0001c0001t0001g0032 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.444+594G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077915 | ||||||
chr4:170078156
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0178others(1): Show | 4 | HG03130.hp1 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+353T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170078156 | ||||||
chr4:170078317
|
A | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 14 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.444+192T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170078317 | ||||||
chr4:170078686
|
A | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-103T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078686 | ||||||
chr4:170078709
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.370-126C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078709 | ||||||
chr4:170078902
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0060a0001c0001t0001g0062 | 4 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-319G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078902 | ||||||
chr4:170078937
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-354G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078937 | ||||||
chr4:170079037
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.370-454T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079037 | ||||||
chr4:170079156
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.370-573G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079156 | ||||||
chr4:170079242
|
C | CG | 5 | a0001c0001t0001g0074a0001c0001t0001g0111a0001c0001t0001g0117others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-660dupC | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079242 | ||||||
chr4:170079467
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0194 | 3 | HG02698.hp1 HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.370-884A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079467 | ||||||
chr4:170079570
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.370-987C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079570 | ||||||
chr4:170079704
|
A | G | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-1121T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079704 | ||||||
chr4:170079774
|
C | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-1191G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079774 | ||||||
chr4:170079810
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.370-1227G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079810 | ||||||
chr4:170079938
|
G | C | 1 | a0001c0001t0001g0044 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.370-1355C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079938 | ||||||
chr4:170079941
|
G | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-1358C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079941 | ||||||
chr4:170080118
|
T | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0048others(5): Show | 14 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.370-1535A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080118 | ||||||
chr4:170080245
|
A | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-1662T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080245 | ||||||
chr4:170080255
|
G | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-1672C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080255 | ||||||
chr4:170080328
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.370-1745C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080328 | ||||||
chr4:170080351
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18941.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.370-1768G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080351 | ||||||
chr4:170080352
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.370-1769C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080352 | ||||||
chr4:170080419
|
G | C | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-1836C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080419 | ||||||
chr4:170080508
|
C | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.370-1925G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080508 | ||||||
chr4:170080514
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.370-1931C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080514 | ||||||
chr4:170080515
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.370-1932G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080515 | ||||||
chr4:170080651
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.370-2068G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080651 | ||||||
chr4:170080674
|
T | C | 1 | a0001c0001t0001g0036 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.370-2091A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080674 | ||||||
chr4:170080681
|
G | T | 1 | a0001c0001t0003g0070 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.370-2098C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080681 | ||||||
chr4:170080739
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.370-2156C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080739 | ||||||
chr4:170080769
|
C | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.370-2186G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080769 | ||||||
chr4:170080884
|
A | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-2301T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080884 | ||||||
chr4:170080970
|
C | A | 1 | a0001c0001t0001g0021 | 3 | HG03041.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.370-2387G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080970 | ||||||
chr4:170080992
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-2409T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080992 | ||||||
chr4:170081124
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.370-2541T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081124 | ||||||
chr4:170081125
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0103 | 7 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-2542G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081125 | ||||||
chr4:170081185
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.370-2602A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081185 | ||||||
chr4:170081237
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.370-2654A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081237 | ||||||
chr4:170081250
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0048a0001c0001t0001g0199others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.370-2667G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081250 | ||||||
chr4:170081251
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.370-2668C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081251 | ||||||
chr4:170081345
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(55): Show | 131 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.370-2762A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081345 | ||||||
chr4:170081550
|
G | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-2967C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081550 | ||||||
chr4:170081820
|
G | A | 8 | a0001c0001t0002g0016a0001c0001t0002g0053a0001c0001t0002g0054others(5): Show | 10 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.370-3237C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081820 | ||||||
chr4:170081879
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.370-3296G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081879 | ||||||
chr4:170081880
|
G | A | 10 | a0001c0001t0001g0052a0001c0001t0002g0016a0001c0001t0002g0053others(7): Show | 13 | HG00323.hp1 HG00639.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.370-3297C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081880 | ||||||
chr4:170081886
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0060a0001c0001t0001g0068others(1): Show | 5 | HG02109.hp2 HG02129.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-3303G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081886 | ||||||
chr4:170081922
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-3339G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081922 | ||||||
chr4:170082043
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.370-3460A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082043 | ||||||
chr4:170082101
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-3518T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082101 | ||||||
chr4:170082161
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.370-3578G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082161 | ||||||
chr4:170082163
|
T | C | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-3580A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082163 | ||||||
chr4:170082176
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0132 | 6 | HG00438.hp1 HG00558.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-3593G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082176 | ||||||
chr4:170082377
|
AT | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-3795delA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082377 | ||||||
chr4:170083015
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.369+4101C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083015 | ||||||
chr4:170083171
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.369+3945T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083171 | ||||||
chr4:170083200
|
C | G | 1 | a0001c0001t0004g0047 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.369+3916G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083200 | ||||||
chr4:170083216
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+3900T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083216 | ||||||
chr4:170083233
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.369+3883C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083233 | ||||||
chr4:170083260
|
G | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+3856C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083260 | ||||||
chr4:170083315
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.369+3801T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083315 | ||||||
chr4:170083346
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0188others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+3770G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083346 | ||||||
chr4:170083347
|
G | A | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+3769C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083347 | ||||||
chr4:170083546
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.369+3570T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083546 | ||||||
chr4:170083572
|
AT | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0188others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+3543delA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083572 | ||||||
chr4:170083573
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.369+3543A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083573 | ||||||
chr4:170083619
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+3497G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083619 | ||||||
chr4:170083937
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.369+3179A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083937 | ||||||
chr4:170084134
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+2982A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084134 | ||||||
chr4:170084197
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0195others(2): Show | 9 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2919C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084197 | ||||||
chr4:170084331
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.369+2785T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084331 | ||||||
chr4:170084406
|
G | T | 1 | a0001c0001t0001g0031 | 2 | NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.369+2710C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084406 | ||||||
chr4:170084540
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.369+2576C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084540 | ||||||
chr4:170084724
|
C | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2392G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084724 | ||||||
chr4:170084796
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.369+2320C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084796 | ||||||
chr4:170084909
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.369+2207A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084909 | ||||||
chr4:170084967
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0195others(2): Show | 9 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2149C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084967 | ||||||
chr4:170084990
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.369+2126A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084990 | ||||||
chr4:170085064
|
T | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(11): Show | 26 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.369+2052A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085064 | ||||||
chr4:170085214
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.369+1902C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085214 | ||||||
chr4:170085289
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.369+1827G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085289 | ||||||
chr4:170085597
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.369+1519C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085597 | ||||||
chr4:170085773
|
G | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+1343C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085773 | ||||||
chr4:170085914
|
TAAGATA | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1196_369+1201d others(8): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085914 | ||||||
chr4:170086008
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0065 | 4 | NA18942.hp1 NA18944.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1108G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086008 | ||||||
chr4:170086107
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.369+1009A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086107 | ||||||
chr4:170086158
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.369+958A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086158 | ||||||
chr4:170086185
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.369+931C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086185 | ||||||
chr4:170086195
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.369+921C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086195 | ||||||
chr4:170086208
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+908G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086208 | ||||||
chr4:170086245
|
C | CA | 3 | a0001c0001t0001g0015a0001c0001t0001g0197a0001c0001t0001g0198 | 6 | HG02559.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+870dupT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086245 | ||||||
chr4:170086317
|
G | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0060a0001c0001t0001g0061others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+799C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086317 | ||||||
chr4:170086353
|
C | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(13): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.369+763G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086353 | ||||||
chr4:170086401
|
GGA | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 17 | HG01109.hp1 HG01358.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.369+713_369+714del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086401 | ||||||
chr4:170086624
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0108 | 2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.369+492G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086624 | ||||||
chr4:170086704
|
G | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.369+412C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086704 | ||||||
chr4:170086907
|
C | A | 1 | a0001c0002t0001g0013 | 5 | NA18941.hp1 NA18991.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+209G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086907 | ||||||
chr4:170086929
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.369+187G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086929 | ||||||
chr4:170086932
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.369+184G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086932 | ||||||
chr4:170086949
|
C | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+167G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086949 | ||||||
chr4:170086953
|
T | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0059 | 3 | HG00408.hp2 NA18950.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.369+163A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086953 | ||||||
chr4:170087373
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.237-125G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087373 | ||||||
chr4:170087538
|
C | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0048others(6): Show | 15 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-290G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087538 | ||||||
chr4:170087538
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0103others(1): Show | 9 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-290G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087538 | ||||||
chr4:170087545
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.237-297C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087545 | ||||||
chr4:170087643
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-395C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087643 | ||||||
chr4:170087679
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.237-431A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087679 | ||||||
chr4:170087750
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.237-502T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087750 | ||||||
chr4:170087751
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0186 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-503A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087751 | ||||||
chr4:170087858
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0048others(6): Show | 15 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+538C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087858 | ||||||
chr4:170087876
|
G | GCTGCTTG others(45): Show |
1 | a0001c0001t0001g0028 | 2 | NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.236+468_236+519dup others(52): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087876 | ||||||
chr4:170087974
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(49): Show | 96 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.236+422G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087974 | ||||||
chr4:170088186
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.236+210G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170088186 | ||||||
chr4:170088209
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(49): Show | 96 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.236+187T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170088209 | ||||||
chr4:170088255
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.236+141A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170088255 | ||||||
chr4:170088637
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-73A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088637 | ||||||
chr4:170088684
|
C | G | 1 | a0001c0001t0007g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-120G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088684 | ||||||
chr4:170088715
|
T | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0046others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-151A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088715 | ||||||
chr4:170088754
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0188others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-190C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088754 | ||||||
chr4:170088835
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.68-271C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088835 | ||||||
chr4:170088936
|
ATGGT | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(14): Show | 30 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-376_68-373delAC others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088936 | ||||||
chr4:170088950
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0048a0001c0001t0001g0199others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-386C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088950 | ||||||
chr4:170088960
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-396G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088960 | ||||||
chr4:170089010
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-446C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089010 | ||||||
chr4:170089163
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67+461C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089163 | ||||||
chr4:170089292
|
G | C | 1 | a0001c0001t0001g0049 | 2 | NA18977.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.67+332C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089292 | ||||||
chr4:170089328
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0059 | 3 | HG00408.hp2 NA18950.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.67+296G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089328 | ||||||
chr4:170089355
|
C | T | 8 | a0001c0001t0001g0052a0001c0001t0002g0016a0001c0001t0002g0053others(5): Show | 10 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+269G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089355 | ||||||
chr4:170089428
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+196G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089428 |