geneid | 29035 |
---|---|
ensemblid | ENSG00000182831.12 |
hgncid | 30103 |
symbol | HAPSTR1 |
name | HUWE1 associated protein modifying stress responses |
refseq_nuc | NM_014117.3 |
refseq_prot | NP_054836.2 |
ensembl_nuc | ENST00000327827.12 |
ensembl_prot | ENSP00000331720.7 |
mane_status | MANE Select |
chr | chr16 |
start | 9091644 |
end | 9121635 |
strand | + |
ver | v1.2 |
region | chr16:9091644-9121635 |
region5000 | chr16:9086644-9126635 |
regionname0 | HAPSTR1_chr16_9091644_9121635 |
regionname5000 | HAPSTR1_chr16_9086644_9126635 |
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 | 275 | 385 | 85 | 68 | 176 | 16 | 38 | 140 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002 | 0/0 | 275 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
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 | 828 | 375 | 82 | 67 | 172 | 16 | 36 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0002 | 0/0 | 828 | 13 | 13 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0003 | 0/0 | 828 | 4 | 0 | 0 | 4 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0004 | 0/0 | 828 | 2 | 0 | 0 | 0 | 0 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0005 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0006 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0007 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
c0008 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5125 | 91 | 2 | 14 | 56 | 7 | 12 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0002 | 0/0 | 5126 | 36 | 0 | 11 | 23 | 2 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0003 | 0/0 | 5127 | 35 | 0 | 6 | 27 | 0 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0004 | 0/0 | 5123 | 22 | 1 | 9 | 1 | 2 | 9 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0005 | 0/0 | 5126 | 20 | 2 | 1 | 11 | 0 | 6 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0006 | 0/0 | 5125 | 20 | 20 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0007 | 0/0 | 5125 | 12 | 12 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0008 | 0/0 | 5126 | 11 | 0 | 1 | 10 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0009 | 0/0 | 5127 | 11 | 10 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0010 | 0/0 | 5126 | 8 | 1 | 4 | 0 | 2 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0011 | 0/0 | 5126 | 8 | 0 | 0 | 8 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0012 | 0/0 | 5126 | 7 | 0 | 0 | 7 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0013 | 0/0 | 5126 | 6 | 4 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0014 | 0/0 | 5127 | 6 | 0 | 0 | 5 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0015 | 0/0 | 5126 | 6 | 0 | 4 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0016 | 0/0 | 5126 | 5 | 5 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0017 | 0/0 | 5119 | 4 | 4 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0018 | 0/0 | 5127 | 3 | 2 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0019 | 0/0 | 5128 | 3 | 0 | 1 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0020 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0021 | 0/0 | 5124 | 3 | 0 | 1 | 1 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0022 | 0/0 | 5127 | 3 | 0 | 0 | 2 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0023 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0024 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0025 | 0/0 | 5124 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0026 | 0/0 | 5126 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0027 | 0/0 | 5125 | 2 | 0 | 0 | 0 | 1 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0028 | 0/0 | 5127 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0029 | 0/0 | 5127 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0030 | 0/0 | 5125 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0031 | 0/0 | 5125 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0032 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0033 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0034 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0035 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0036 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0037 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0038 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0039 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0040 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0041 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0042 | 0/0 | 5124 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0043 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0044 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0045 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0046 | 0/1 | 5123 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0047 | 0/0 | 5123 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0048 | 0/0 | 5123 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0049 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0050 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0051 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0052 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0053 | 0/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0054 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0055 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0056 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0057 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0058 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0059 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0060 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0061 | 0/0 | 5128 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0062 | 0/0 | 5128 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0063 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0064 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0065 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0066 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0067 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0068 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0069 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0070 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0071 | 1/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0072 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0073 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0074 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0075 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0076 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0077 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0078 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0079 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0080 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0081 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0082 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0083 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0084 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0085 | 0/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
t0086 | 0/0 | 5120 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
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 | 23 | 2 | 5 | 6 | 3 | 7 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0002 | 0/0 | 21 | 0 | 3 | 12 | 4 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0003 | 0/0 | 15 | 0 | 2 | 12 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0004 | 0/0 | 13 | 0 | 3 | 10 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0005 | 0/0 | 9 | 0 | 5 | 3 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0006 | 0/0 | 9 | 0 | 5 | 0 | 1 | 3 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0008 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0011 | 0/0 | 6 | 1 | 2 | 1 | 1 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0017 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0026 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0029 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
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 | 828 | 375 | 82 | 67 | 172 | 16 | 36 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0003 | 0/0 | 828 | 4 | 0 | 0 | 4 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0004 | 0/0 | 828 | 2 | 0 | 0 | 0 | 0 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0005 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0006 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0007 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0008 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002c0002 | 0/0 | 828 | 13 | 13 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5952 | 88 | 2 | 14 | 54 | 7 | 11 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0002 | 0/0 | 5953 | 36 | 0 | 11 | 23 | 2 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0003 | 0/0 | 5954 | 35 | 0 | 6 | 27 | 0 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0004 | 0/0 | 5950 | 21 | 1 | 8 | 1 | 2 | 9 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0005 | 0/0 | 5953 | 20 | 2 | 1 | 11 | 0 | 6 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0006 | 0/0 | 5952 | 20 | 20 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0007 | 0/0 | 5952 | 12 | 12 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0008 | 0/0 | 5953 | 11 | 0 | 1 | 10 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0009 | 0/0 | 5954 | 10 | 9 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0010 | 0/0 | 5953 | 8 | 1 | 4 | 0 | 2 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0011 | 0/0 | 5953 | 8 | 0 | 0 | 8 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0012 | 0/0 | 5953 | 7 | 0 | 0 | 7 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0013 | 0/0 | 5953 | 6 | 4 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0014 | 0/0 | 5954 | 6 | 0 | 0 | 5 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0015 | 0/0 | 5953 | 6 | 0 | 4 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0018 | 0/0 | 5954 | 3 | 2 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0019 | 0/0 | 5955 | 3 | 0 | 1 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0020 | 0/0 | 5954 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0021 | 0/0 | 5951 | 2 | 0 | 1 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0022 | 0/0 | 5954 | 3 | 0 | 0 | 2 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0023 | 0/0 | 5952 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0024 | 0/0 | 5952 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0025 | 0/0 | 5951 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0026 | 0/0 | 5953 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0027 | 0/0 | 5952 | 2 | 0 | 0 | 0 | 1 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0028 | 0/0 | 5954 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0029 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0031 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0032 | 0/0 | 5952 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0034 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0035 | 0/0 | 5953 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0036 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0037 | 0/0 | 5953 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0038 | 0/0 | 5954 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0039 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0041 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0042 | 0/0 | 5951 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0043 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0045 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0046 | 0/1 | 5950 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0047 | 0/0 | 5950 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0048 | 0/0 | 5950 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0049 | 0/0 | 5953 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0050 | 0/0 | 5955 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0051 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0052 | 0/0 | 5954 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0053 | 0/0 | 5952 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0054 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0055 | 0/0 | 5954 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0056 | 0/0 | 5954 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0057 | 0/0 | 5954 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0058 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0059 | 0/0 | 5956 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0060 | 0/0 | 5954 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0061 | 0/0 | 5955 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0062 | 0/0 | 5955 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0063 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0064 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0065 | 0/0 | 5955 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0066 | 0/0 | 5953 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0067 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0068 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0069 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0070 | 0/0 | 5952 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0071 | 1/0 | 5952 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0072 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0073 | 0/0 | 5953 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0074 | 0/0 | 5952 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0075 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0076 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0077 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0078 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0079 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0080 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0081 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0082 | 0/0 | 5953 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0083 | 0/0 | 5953 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0084 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0001t0085 | 0/0 | 5952 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0003t0001 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0003t0030 | 0/0 | 5952 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0004t0001 | 0/0 | 5952 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0004t0021 | 0/0 | 5951 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0005t0044 | 0/0 | 5953 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0006t0029 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0007t0004 | 0/0 | 5950 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0001c0008t0009 | 0/0 | 5954 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002c0002t0016 | 0/0 | 5953 | 5 | 5 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002c0002t0017 | 0/0 | 5946 | 4 | 4 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002c0002t0033 | 0/0 | 5952 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002c0002t0040 | 0/0 | 5952 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
a0002c0002t0086 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | copy fasta | chr16 | 9086644 | 9126635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 19 | 0 | 2 | 11 | 4 | 2 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0011 | 0/0 | 5 | 1 | 1 | 1 | 1 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0004 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0003 | 0/0 | 13 | 0 | 2 | 10 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0006 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0001 | 0/0 | 13 | 1 | 1 | 6 | 0 | 5 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0008g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0009g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0009g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0010g0001 | 0/0 | 7 | 1 | 3 | 0 | 2 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0010g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0011g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0011g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0012g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0013g0029 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0013g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0014g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0014g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0015g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0015g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0015g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0015g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0015g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0018g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0018g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0019g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0019g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0020g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0021g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0021g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0022g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0022g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0022g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0023g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0024g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0025g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0025g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0026g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0026g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0027g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0028g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0029g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0031g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0031g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0032g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0032g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0034g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0035g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0036g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0037g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0038g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0039g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0041g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0042g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0043g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0045g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0046g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0047g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0048g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0049g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0050g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0051g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0052g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0053g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0054g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0055g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0056g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0057g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0058g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0059g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0060g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0061g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0062g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0063g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0064g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0065g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0066g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0067g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0068g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0069g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0070g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0071g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0072g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0073g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0074g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0075g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0076g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0077g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0078g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0079g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0080g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0081g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0082g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0083g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0084g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0001t0085g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0003t0030g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0003t0030g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0004t0021g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0005t0044g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0006t0029g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0007t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0001c0008t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0016g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0017g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0017g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0033g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0040g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
a0002c0002t0086g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0105 | EUR | GBR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | GBR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00280 | hp2 | a0001 | c0001 | t0014 | g0001 | EUR | FIN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | FIN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00597 | hp1 | a0001 | c0001 | t0011 | g0189 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00639 | hp2 | a0001 | c0001 | t0063 | g0080 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00642 | hp1 | a0001 | c0001 | t0039 | g0058 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00642 | hp2 | a0001 | c0001 | t0049 | g0001 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | CHS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01074 | hp1 | a0001 | c0001 | t0010 | g0099 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01106 | hp1 | a0001 | c0001 | t0042 | g0006 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01106 | hp2 | a0001 | c0001 | t0036 | g0061 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01109 | hp1 | a0001 | c0001 | t0018 | g0160 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0029 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01169 | hp1 | a0001 | c0001 | t0013 | g0029 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01169 | hp2 | a0001 | c0001 | t0015 | g0077 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01175 | hp1 | a0001 | c0001 | t0015 | g0005 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01192 | hp1 | a0001 | c0001 | t0037 | g0005 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0161 | AMR | PUR | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01255 | hp1 | a0001 | c0001 | t0021 | g0005 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01346 | hp2 | a0001 | c0001 | t0019 | g0126 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01358 | hp2 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01361 | hp1 | a0001 | c0007 | t0004 | g0179 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01361 | hp2 | a0001 | c0001 | t0015 | g0005 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01433 | hp1 | a0001 | c0001 | t0074 | g0011 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01496 | hp2 | a0001 | c0001 | t0072 | g0084 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0001 | EUR | IBS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0001 | EUR | IBS | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01978 | hp2 | a0001 | c0001 | t0057 | g0170 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01993 | hp1 | a0001 | c0001 | t0015 | g0002 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01993 | hp2 | a0001 | c0001 | t0035 | g0082 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02040 | hp1 | a0001 | c0001 | t0011 | g0188 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02055 | hp1 | a0002 | c0002 | t0086 | g0009 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02055 | hp2 | a0001 | c0001 | t0028 | g0036 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02071 | hp2 | a0001 | c0001 | t0008 | g0120 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02074 | hp1 | a0001 | c0001 | t0041 | g0007 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02132 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | KHV | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02145 | hp1 | a0001 | c0001 | t0043 | g0015 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02145 | hp2 | a0002 | c0002 | t0017 | g0115 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02148 | hp1 | a0001 | c0001 | t0055 | g0171 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02155 | hp1 | a0001 | c0001 | t0070 | g0100 | EAS | CDX | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CDX | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02257 | hp1 | a0002 | c0002 | t0016 | g0152 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02257 | hp2 | a0001 | c0008 | t0009 | g0177 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02280 | hp1 | a0001 | c0001 | t0078 | g0014 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02280 | hp2 | a0001 | c0001 | t0028 | g0036 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02451 | hp1 | a0002 | c0002 | t0017 | g0009 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0163 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02572 | hp1 | a0001 | c0001 | t0024 | g0040 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0198 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02615 | hp2 | a0001 | c0001 | t0023 | g0051 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02622 | hp1 | a0001 | c0001 | t0081 | g0098 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02630 | hp1 | a0002 | c0002 | t0016 | g0023 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0142 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02647 | hp2 | a0001 | c0001 | t0023 | g0051 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02683 | hp1 | a0001 | c0004 | t0001 | g0086 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02698 | hp1 | a0001 | c0001 | t0027 | g0032 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02723 | hp1 | a0001 | c0001 | t0084 | g0149 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02723 | hp2 | a0001 | c0001 | t0054 | g0044 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02809 | hp2 | a0002 | c0002 | t0016 | g0009 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02818 | hp1 | a0002 | c0002 | t0016 | g0023 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0158 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0043 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0148 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0140 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02922 | hp2 | a0001 | c0001 | t0018 | g0024 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02965 | hp2 | a0002 | c0002 | t0033 | g0009 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02970 | hp1 | a0001 | c0001 | t0064 | g0156 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02970 | hp2 | a0001 | c0001 | t0050 | g0024 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02976 | hp1 | a0001 | c0006 | t0029 | g0165 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02976 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03041 | hp1 | a0001 | c0001 | t0024 | g0107 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03098 | hp2 | a0001 | c0001 | t0018 | g0159 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03139 | hp2 | a0001 | c0001 | t0080 | g0211 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03195 | hp1 | a0002 | c0002 | t0016 | g0023 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03209 | hp1 | a0002 | c0002 | t0017 | g0009 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03209 | hp2 | a0001 | c0001 | t0076 | g0097 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03225 | hp2 | a0001 | c0001 | t0075 | g0096 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03453 | hp2 | a0001 | c0001 | t0051 | g0024 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03486 | hp1 | a0001 | c0001 | t0020 | g0043 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03486 | hp2 | a0002 | c0002 | t0040 | g0123 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03491 | hp1 | a0001 | c0001 | t0085 | g0083 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03516 | hp2 | a0001 | c0001 | t0065 | g0180 | AFR | ESN | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03540 | hp1 | a0002 | c0002 | t0017 | g0009 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0138 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03669 | hp1 | a0001 | c0001 | t0083 | g0192 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0144 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0206 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03831 | hp1 | a0001 | c0001 | t0047 | g0145 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03831 | hp2 | a0001 | c0001 | t0082 | g0001 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03834 | hp1 | a0001 | c0004 | t0021 | g0070 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0146 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04184 | hp2 | a0001 | c0001 | t0048 | g0049 | SAS | BEB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04199 | hp2 | a0001 | c0001 | t0053 | g0052 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0001 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0154 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18522 | hp1 | a0001 | c0005 | t0044 | g0214 | AFR | YRI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18522 | hp2 | a0001 | c0001 | t0034 | g0215 | AFR | YRI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18747 | hp1 | a0001 | c0001 | t0022 | g0028 | EAS | CHB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | CHB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | YRI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0164 | AFR | YRI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18939 | hp2 | a0001 | c0001 | t0008 | g0117 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18940 | hp1 | a0001 | c0001 | t0022 | g0017 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18940 | hp2 | a0001 | c0001 | t0014 | g0022 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18946 | hp1 | a0001 | c0003 | t0030 | g0212 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18946 | hp2 | a0001 | c0001 | t0045 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18948 | hp1 | a0001 | c0001 | t0056 | g0129 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18949 | hp2 | a0001 | c0001 | t0014 | g0133 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18950 | hp1 | a0001 | c0001 | t0025 | g0079 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18950 | hp2 | a0001 | c0001 | t0014 | g0134 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18953 | hp1 | a0001 | c0001 | t0025 | g0078 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18953 | hp2 | a0001 | c0001 | t0012 | g0071 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18962 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18962 | hp2 | a0001 | c0001 | t0069 | g0054 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18963 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18963 | hp2 | a0001 | c0001 | t0031 | g0205 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18968 | hp2 | a0001 | c0001 | t0067 | g0210 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18972 | hp1 | a0001 | c0001 | t0019 | g0021 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18973 | hp1 | a0001 | c0001 | t0066 | g0005 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18973 | hp2 | a0001 | c0001 | t0015 | g0183 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18975 | hp1 | a0001 | c0001 | t0062 | g0045 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18975 | hp2 | a0001 | c0001 | t0012 | g0209 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18977 | hp1 | a0001 | c0001 | t0060 | g0031 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18977 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18989 | hp1 | a0001 | c0001 | t0052 | g0114 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18989 | hp2 | a0001 | c0001 | t0015 | g0010 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18990 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18990 | hp2 | a0001 | c0001 | t0014 | g0022 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18994 | hp1 | a0001 | c0001 | t0031 | g0207 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18995 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18999 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19002 | hp1 | a0001 | c0001 | t0011 | g0190 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19007 | hp2 | a0001 | c0001 | t0014 | g0022 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19010 | hp1 | a0001 | c0001 | t0019 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19011 | hp2 | a0001 | c0003 | t0030 | g0050 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19030 | hp1 | a0001 | c0001 | t0020 | g0175 | AFR | LWK | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0169 | AFR | LWK | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19043 | hp1 | a0001 | c0001 | t0068 | g0044 | AFR | LWK | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | LWK | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19056 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19057 | hp1 | a0001 | c0001 | t0021 | g0092 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19058 | hp1 | a0001 | c0001 | t0061 | g0031 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19060 | hp2 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19062 | hp1 | a0001 | c0001 | t0038 | g0037 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19066 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19066 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19076 | hp2 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19079 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19083 | hp2 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19086 | hp1 | a0001 | c0001 | t0058 | g0193 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19086 | hp2 | a0001 | c0001 | t0026 | g0008 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19088 | hp2 | a0001 | c0001 | t0026 | g0122 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19089 | hp2 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19240 | hp1 | a0001 | c0001 | t0032 | g0053 | AFR | YRI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | YRI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0178 | AFR | ASW | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20752 | hp1 | a0001 | c0001 | t0027 | g0032 | EUR | TSI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20752 | hp2 | a0001 | c0001 | t0022 | g0026 | EUR | TSI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG01123 | hp2 | a0001 | c0001 | t0073 | g0202 | AMR | CLM | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02109 | hp2 | a0002 | c0002 | t0033 | g0009 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG02559 | hp2 | a0001 | c0001 | t0077 | g0137 | AFR | ACB | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG03471 | hp2 | a0001 | c0001 | t0079 | g0150 | AFR | MSL | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG06807 | hp1 | a0001 | c0001 | t0029 | g0119 | AFR | USA | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | USA | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA18955 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20300 | hp1 | a0001 | c0001 | t0032 | g0204 | AFR | USA | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA20300 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | USA | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | LWK | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
NA21309 | hp2 | a0001 | c0001 | t0059 | g0012 | AFR | LWK | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0046 | g0113 | REF | REF | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0071 | g0056 | REF | REF | HAPSTR1_chr16_9086644_9126635 | HAPSTR1 | chr16 | 9086644 | 9126635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:9116746
|
A | G | 1 | a0002 | 13 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
missense_variant | MODERATE | c.662A>G | p.Asn221Ser | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1063/5952 | 662/828 | 221/275 | chr16 | 9116746 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:9092068
|
C | T | 1 | a0001c0008 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.24C>T | p.Gly8Gly | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 425/5952 | 24/828 | 8/275 | chr16 | 9092068 | ||
chr16:9092071
|
G | A | 1 | a0001c0004 | 2 | HG02683.hp1 HG03834.hp1 |
synonymous_variant | LOW | c.27G>A | p.Glu9Glu | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 428/5952 | 27/828 | 9/275 | chr16 | 9092071 | ||
chr16:9092074
|
C | T | 1 | a0001c0007 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.30C>T | p.Ala10Ala | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 431/5952 | 30/828 | 10/275 | chr16 | 9092074 | ||
chr16:9092156
|
C | T | 1 | a0001c0003 | 4 | NA18945.hp2 NA18946.hp1 NA19011.hp2 others(1): Show |
synonymous_variant | LOW | c.112C>T | p.Leu38Leu | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 513/5952 | 112/828 | 38/275 | chr16 | 9092156 | ||
chr16:9092958
|
C | G | 1 | a0001c0006 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.264C>G | p.Val88Val | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/4 | 665/5952 | 264/828 | 88/275 | chr16 | 9092958 | ||
chr16:9092961
|
C | T | 1 | a0001c0005 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.267C>T | p.Pro89Pro | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/4 | 668/5952 | 267/828 | 89/275 | chr16 | 9092961 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:9091652
|
T | G | 1 | a0001c0001t0034 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-393T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 393 | chr16 | 9091652 | |||||
chr16:9091683
|
G | T | 4 | a0002c0002t0016a0002c0002t0017a0002c0002t0033others(1): Show | 12 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-362G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 362 | chr16 | 9091683 | |||||
chr16:9091742
|
G | T | 1 | a0001c0001t0085 | 1 | HG03491.hp1 | 5_prime_UTR_variant | MODIFIER | c.-303G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 303 | chr16 | 9091742 | |||||
chr16:9091761
|
C | T | 1 | a0001c0001t0084 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 284 | chr16 | 9091761 | |||||
chr16:9091781
|
G | A | 1 | a0001c0001t0023 | 2 | HG02615.hp2 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-264G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 264 | chr16 | 9091781 | |||||
chr16:9091825
|
G | T | 1 | a0001c0001t0083 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-220G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 220 | chr16 | 9091825 | |||||
chr16:9091929
|
G | A | 1 | a0001c0001t0035 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 116 | chr16 | 9091929 | |||||
chr16:9092031
|
G | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG01106.hp2 HG01192.hp1 |
5_prime_UTR_variant | MODIFIER | c.-14G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/4 | 14 | chr16 | 9092031 | |||||
chr16:9116919
|
A | G | 1 | a0001c0001t0082 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 7 | chr16 | 9116919 | |||||
chr16:9116974
|
A | G | 1 | a0001c0001t0081 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 62 | chr16 | 9116974 | |||||
chr16:9117054
|
G | A | 1 | a0001c0001t0038 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 142 | chr16 | 9117054 | |||||
chr16:9117260
|
C | CT | 4 | a0001c0001t0012a0001c0001t0022a0001c0001t0035others(1): Show | 12 | HG01192.hp1 HG01993.hp2 NA18747.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*361dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 362 | INFO_REALIGN_3_PRIME | chr16 | 9117260 | ||||
chr16:9117260
|
CT | C | 15 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(12): Show | 64 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*361delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 361 | INFO_REALIGN_3_PRIME | chr16 | 9117260 | ||||
chr16:9117260
|
CTT | C | 5 | a0002c0002t0016a0002c0002t0017a0002c0002t0033others(2): Show | 13 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*360_*361delTT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 360 | INFO_REALIGN_3_PRIME | chr16 | 9117260 | ||||
chr16:9117262
|
T | G | 1 | a0001c0001t0039 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 350 | chr16 | 9117262 | |||||
chr16:9117273
|
T | G | 1 | a0001c0001t0041 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*361T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 361 | chr16 | 9117273 | |||||
chr16:9117390
|
G | T | 1 | a0001c0001t0032 | 2 | NA19240.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*478G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 478 | chr16 | 9117390 | |||||
chr16:9117396
|
A | G | 1 | a0001c0001t0048 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 484 | chr16 | 9117396 | |||||
chr16:9117438
|
G | C | 2 | a0001c0001t0010a0001c0001t0049 | 9 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*526G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 526 | chr16 | 9117438 | |||||
chr16:9117516
|
A | G | 1 | a0001c0001t0034 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 604 | chr16 | 9117516 | |||||
chr16:9117670
|
A | G | 5 | a0001c0001t0006a0001c0001t0077a0001c0001t0078others(2): Show | 24 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*758A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 758 | chr16 | 9117670 | |||||
chr16:9117738
|
C | G | 3 | a0001c0001t0075a0001c0001t0076a0001c0001t0081 | 3 | HG02622.hp1 HG03209.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*826C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 826 | chr16 | 9117738 | |||||
chr16:9117771
|
TAGTGAG | T | 2 | a0002c0002t0017a0002c0002t0086 | 5 | HG02055.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*862_*867delTGAGAG | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 862 | INFO_REALIGN_3_PRIME | chr16 | 9117771 | ||||
chr16:9117802
|
G | A | 3 | a0001c0001t0018a0001c0001t0050a0001c0001t0051 | 5 | HG01109.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*890G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 890 | chr16 | 9117802 | |||||
chr16:9117866
|
G | A | 2 | a0001c0001t0011a0001c0001t0052 | 9 | HG00597.hp1 HG02040.hp1 HG02132.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 954 | chr16 | 9117866 | |||||
chr16:9117992
|
A | T | 1 | a0001c0001t0074 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1080A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1080 | chr16 | 9117992 | |||||
chr16:9118005
|
T | C | 1 | a0001c0001t0053 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1093T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1093 | chr16 | 9118005 | |||||
chr16:9118007
|
G | C | 1 | a0001c0001t0049 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1095 | chr16 | 9118007 | |||||
chr16:9118059
|
A | C | 1 | a0001c0001t0051 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1147 | chr16 | 9118059 | |||||
chr16:9118061
|
T | C | 1 | a0001c0001t0035 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1149T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1149 | chr16 | 9118061 | |||||
chr16:9118124
|
T | C | 1 | a0001c0001t0054 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1212 | chr16 | 9118124 | |||||
chr16:9118229
|
A | G | 1 | a0001c0001t0047 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1317 | chr16 | 9118229 | |||||
chr16:9118312
|
C | G | 1 | a0001c0001t0080 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1400C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1400 | chr16 | 9118312 | |||||
chr16:9118435
|
G | A | 1 | a0001c0001t0032 | 2 | NA19240.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1523G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1523 | chr16 | 9118435 | |||||
chr16:9118473
|
A | G | 1 | a0001c0001t0026 | 2 | NA19086.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1561A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1561 | chr16 | 9118473 | |||||
chr16:9118494
|
G | A | 1 | a0001c0001t0024 | 2 | HG02572.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1582G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1582 | chr16 | 9118494 | |||||
chr16:9118504
|
C | A | 1 | a0001c0001t0027 | 2 | HG02698.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1592C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1592 | chr16 | 9118504 | |||||
chr16:9118742
|
C | T | 2 | a0001c0001t0072a0001c0001t0073 | 2 | HG01123.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1830C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 1830 | chr16 | 9118742 | |||||
chr16:9119102
|
G | A | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
3_prime_UTR_variant | MODIFIER | c.*2190G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2190 | chr16 | 9119102 | |||||
chr16:9119130
|
T | C | 55 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(52): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*2218T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2218 | chr16 | 9119130 | |||||
chr16:9119182
|
C | G | 1 | a0001c0001t0070 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2270C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2270 | chr16 | 9119182 | |||||
chr16:9119184
|
G | A | 1 | a0001c0001t0063 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2272 | chr16 | 9119184 | |||||
chr16:9119284
|
C | G | 1 | a0001c0001t0046 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2372C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2372 | chr16 | 9119284 | |||||
chr16:9119340
|
A | G | 1 | a0001c0001t0034 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2428A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2428 | chr16 | 9119340 | |||||
chr16:9119365
|
G | A | 1 | a0001c0001t0055 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2453G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2453 | chr16 | 9119365 | |||||
chr16:9119445
|
T | A | 1 | a0001c0001t0056 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2533T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2533 | chr16 | 9119445 | |||||
chr16:9119562
|
A | C | 30 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(27): Show | 116 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2650A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2650 | chr16 | 9119562 | |||||
chr16:9119584
|
T | A | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
3_prime_UTR_variant | MODIFIER | c.*2672T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 2672 | chr16 | 9119584 | |||||
chr16:9120023
|
A | C | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(42): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*3111A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3111 | chr16 | 9120023 | |||||
chr16:9120044
|
C | A | 1 | a0001c0003t0030 | 2 | NA18946.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3132C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3132 | chr16 | 9120044 | |||||
chr16:9120511
|
GT | G | 56 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(53): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3601delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3601 | INFO_REALIGN_3_PRIME | chr16 | 9120511 | ||||
chr16:9120528
|
G | A | 1 | a0001c0001t0031 | 2 | NA18963.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3616G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3616 | chr16 | 9120528 | |||||
chr16:9120673
|
C | CT | 25 | a0001c0001t0003a0001c0001t0008a0001c0001t0013others(22): Show | 92 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*3783dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3784 | INFO_REALIGN_3_PRIME | chr16 | 9120673 | ||||
chr16:9120673
|
C | CTT | 6 | a0001c0001t0019a0001c0001t0059a0001c0001t0062others(3): Show | 12 | HG01346.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3782_*3783dupTT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3784 | INFO_REALIGN_3_PRIME | chr16 | 9120673 | ||||
chr16:9120673
|
CT | C | 8 | a0001c0001t0006a0001c0001t0021a0001c0001t0034others(5): Show | 28 | HG01106.hp1 HG01255.hp1 HG01884.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3783delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3783 | INFO_REALIGN_3_PRIME | chr16 | 9120673 | ||||
chr16:9120673
|
CTT | C | 5 | a0001c0001t0004a0001c0001t0046a0001c0001t0047others(2): Show | 25 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3782_*3783delTT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3782 | INFO_REALIGN_3_PRIME | chr16 | 9120673 | ||||
chr16:9120695
|
T | G | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0022others(2): Show | 49 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3783T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3783 | chr16 | 9120695 | |||||
chr16:9120714
|
C | G | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0022others(2): Show | 49 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3802C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3802 | chr16 | 9120714 | |||||
chr16:9120741
|
G | A | 3 | a0001c0001t0007a0001c0001t0024a0001c0001t0043 | 15 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3829G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 3829 | chr16 | 9120741 | |||||
chr16:9120974
|
G | T | 56 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(53): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*4062G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4062 | chr16 | 9120974 | |||||
chr16:9121083
|
A | G | 37 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(34): Show | 130 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4171A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4171 | chr16 | 9121083 | |||||
chr16:9121208
|
C | T | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0022others(2): Show | 49 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4296C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4296 | chr16 | 9121208 | |||||
chr16:9121286
|
T | C | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*4374T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4374 | chr16 | 9121286 | |||||
chr16:9121308
|
A | G | 64 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(61): Show | 264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*4396A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4396 | chr16 | 9121308 | |||||
chr16:9121512
|
C | G | 1 | a0002c0002t0040 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4600C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4600 | chr16 | 9121512 | |||||
chr16:9121515
|
G | A | 1 | a0001c0001t0048 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4603G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4603 | chr16 | 9121515 | |||||
chr16:9121519
|
G | A | 1 | a0001c0001t0077 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4607G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4607 | chr16 | 9121519 | |||||
chr16:9121574
|
G | C | 3 | a0001c0001t0008a0001c0001t0026a0001c0001t0057 | 14 | HG01928.hp2 HG01978.hp2 HG02071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4662G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4662 | chr16 | 9121574 | |||||
chr16:9121578
|
T | TCA | 64 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(61): Show | 264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*4666_*4667insCA | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4667 | chr16 | 9121578 | |||||
chr16:9121624
|
A | T | 19 | a0001c0001t0003a0001c0001t0008a0001c0001t0013others(16): Show | 79 | HG00438.hp2 HG00673.hp2 HG01070.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4712A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 4/4 | 4712 | chr16 | 9121624 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:9092335
|
A | G | 3 | a0001c0001t0023g0051a0001c0001t0034g0215a0001c0005t0044g0214 | 4 | HG02615.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+65A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092335 | ||||||
chr16:9092375
|
G | A | 1 | a0001c0005t0044g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.226+105G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092375 | ||||||
chr16:9092383
|
G | T | 4 | a0001c0003t0001g0050a0001c0003t0001g0213a0001c0003t0030g0050others(1): Show | 4 | NA18945.hp2 NA18946.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+113G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092383 | ||||||
chr16:9092418
|
C | T | 1 | a0001c0001t0080g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.226+148C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092418 | ||||||
chr16:9092424
|
G | A | 1 | a0001c0001t0053g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.226+154G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092424 | ||||||
chr16:9092435
|
C | T | 1 | a0001c0001t0067g0210 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.226+165C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092435 | ||||||
chr16:9092455
|
G | A | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.226+185G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092455 | ||||||
chr16:9092548
|
C | T | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.226+278C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092548 | ||||||
chr16:9092551
|
C | T | 1 | a0001c0001t0012g0209 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.226+281C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092551 | ||||||
chr16:9092562
|
C | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(232): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.226+292C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092562 | ||||||
chr16:9092569
|
G | T | 15 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(12): Show | 33 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.226+299G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092569 | ||||||
chr16:9092616
|
C | G | 3 | a0001c0001t0004g0049a0001c0001t0004g0198a0001c0001t0048g0049 | 3 | HG02602.hp1 HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.227-305C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092616 | ||||||
chr16:9092653
|
CA | C | 27 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0184others(24): Show | 50 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.227-267delA | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092653 | ||||||
chr16:9092654
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0048a0001c0001t0001g0196others(2): Show | 11 | HG00544.hp1 HG01261.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.227-267A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092654 | ||||||
chr16:9092654
|
A | T | 1 | a0001c0001t0005g0208 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.227-267A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092654 | ||||||
chr16:9092707
|
C | T | 27 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0002g0004others(24): Show | 50 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.227-214C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092707 | ||||||
chr16:9092751
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.227-170G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092751 | ||||||
chr16:9092771
|
A | T | 1 | a0001c0001t0065g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-150A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092771 | ||||||
chr16:9092833
|
C | G | 1 | a0001c0007t0004g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.227-88C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092833 | ||||||
chr16:9092850
|
C | G | 1 | a0001c0001t0013g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.227-71C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092850 | ||||||
chr16:9092852
|
C | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.227-69C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092852 | ||||||
chr16:9092878
|
C | G | 148 | a0001c0001t0001g0153a0001c0001t0001g0168a0001c0001t0002g0004others(145): Show | 224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.227-43C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | chr16 | 9092878 | ||||||
chr16:9092892
|
G | GT | 28 | a0001c0001t0001g0013a0001c0001t0001g0063a0001c0001t0001g0064others(25): Show | 33 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.227-15dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 9092892 | |||||
chr16:9093053
|
G | T | 1 | a0001c0001t0070g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.307+52G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093053 | ||||||
chr16:9093147
|
A | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307+146A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093147 | ||||||
chr16:9093201
|
G | A | 1 | a0001c0001t0069g0054 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.307+200G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093201 | ||||||
chr16:9093250
|
G | A | 1 | a0001c0001t0013g0034 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.307+249G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093250 | ||||||
chr16:9093304
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.307+303C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093304 | ||||||
chr16:9093335
|
A | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(247): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.307+334A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093335 | ||||||
chr16:9093335
|
A | G | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.307+334A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093335 | ||||||
chr16:9093342
|
T | A | 2 | a0001c0001t0023g0051a0001c0001t0034g0215 | 3 | HG02615.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.307+341T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093342 | ||||||
chr16:9093369
|
G | T | 2 | a0001c0001t0023g0051a0001c0001t0034g0215 | 3 | HG02615.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.307+368G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093369 | ||||||
chr16:9093399
|
C | T | 22 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(19): Show | 42 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.307+398C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093399 | ||||||
chr16:9093421
|
G | A | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.307+420G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093421 | ||||||
chr16:9093517
|
C | G | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.307+516C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093517 | ||||||
chr16:9093618
|
A | G | 21 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(18): Show | 41 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.307+617A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093618 | ||||||
chr16:9093633
|
T | C | 23 | a0001c0001t0005g0001a0001c0001t0005g0104a0001c0001t0005g0199others(20): Show | 43 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.307+632T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093633 | ||||||
chr16:9093864
|
T | C | 171 | a0001c0001t0001g0068a0001c0001t0001g0153a0001c0001t0002g0004others(168): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.307+863T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093864 | ||||||
chr16:9093995
|
A | G | 1 | a0001c0001t0004g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.307+994A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9093995 | ||||||
chr16:9094028
|
G | T | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.307+1027G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094028 | ||||||
chr16:9094284
|
G | T | 4 | a0001c0001t0001g0068a0001c0001t0003g0046a0001c0001t0003g0166others(1): Show | 5 | NA18984.hp2 NA19054.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.307+1283G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094284 | ||||||
chr16:9094360
|
G | C | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.307+1359G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094360 | ||||||
chr16:9094465
|
C | G | 1 | a0001c0006t0029g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.307+1464C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094465 | ||||||
chr16:9094487
|
AT | A | 9 | a0001c0001t0002g0185a0001c0001t0006g0035a0001c0001t0006g0106others(6): Show | 10 | HG01256.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.307+1498delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9094487 | |||||
chr16:9094494
|
T | C | 1 | a0001c0001t0004g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.307+1493T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094494 | ||||||
chr16:9094499
|
T | C | 1 | a0001c0001t0046g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.307+1498T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094499 | ||||||
chr16:9094520
|
C | T | 2 | a0001c0001t0054g0044a0001c0001t0068g0044 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.307+1519C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094520 | ||||||
chr16:9094596
|
G | C | 21 | a0001c0001t0005g0001a0001c0001t0005g0104a0001c0001t0005g0199others(18): Show | 41 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.307+1595G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094596 | ||||||
chr16:9094733
|
A | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307+1732A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094733 | ||||||
chr16:9094807
|
T | C | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307+1806T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094807 | ||||||
chr16:9094896
|
A | G | 1 | a0001c0001t0006g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.307+1895A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094896 | ||||||
chr16:9094924
|
A | T | 14 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(11): Show | 19 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.307+1923A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094924 | ||||||
chr16:9094938
|
A | T | 1 | a0001c0001t0003g0157 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.307+1937A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9094938 | ||||||
chr16:9095072
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.307+2071A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095072 | ||||||
chr16:9095111
|
C | G | 21 | a0001c0001t0005g0001a0001c0001t0005g0104a0001c0001t0005g0199others(18): Show | 41 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.307+2110C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095111 | ||||||
chr16:9095161
|
C | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.307+2160C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095161 | ||||||
chr16:9095210
|
A | C | 1 | a0001c0001t0064g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.307+2209A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095210 | ||||||
chr16:9095210
|
A | G | 1 | a0001c0001t0080g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307+2209A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095210 | ||||||
chr16:9095291
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.307+2290T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095291 | ||||||
chr16:9095355
|
A | G | 1 | a0001c0001t0003g0155 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.307+2354A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095355 | ||||||
chr16:9095420
|
T | A | 13 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(10): Show | 18 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.307+2419T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095420 | ||||||
chr16:9095447
|
G | C | 1 | a0001c0001t0006g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307+2446G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095447 | ||||||
chr16:9095506
|
A | C | 14 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(11): Show | 19 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.307+2505A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095506 | ||||||
chr16:9095667
|
C | T | 19 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(16): Show | 39 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.307+2666C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095667 | ||||||
chr16:9095730
|
G | A | 14 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(11): Show | 19 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.307+2729G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095730 | ||||||
chr16:9095852
|
T | C | 1 | a0001c0004t0021g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.307+2851T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095852 | ||||||
chr16:9095863
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.307+2862G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095863 | ||||||
chr16:9095878
|
TACTG | T | 19 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(16): Show | 39 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.307+2882_307+2885d others(6): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9095878 | |||||
chr16:9095902
|
A | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307+2901A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095902 | ||||||
chr16:9095959
|
A | AT | 19 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(16): Show | 39 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.307+2964dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9095959 | |||||
chr16:9095966
|
G | C | 19 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(16): Show | 39 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.307+2965G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9095966 | ||||||
chr16:9096099
|
C | G | 1 | a0001c0001t0004g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.307+3098C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096099 | ||||||
chr16:9096166
|
T | G | 13 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(10): Show | 18 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.307+3165T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096166 | ||||||
chr16:9096355
|
T | C | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.307+3354T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096355 | ||||||
chr16:9096377
|
G | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.307+3376G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096377 | ||||||
chr16:9096381
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.307+3380A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096381 | ||||||
chr16:9096390
|
TTCA | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(11): Show | 32 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.307+3392_307+3394d others(5): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9096390 | |||||
chr16:9096418
|
T | C | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307+3417T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096418 | ||||||
chr16:9096433
|
C | G | 1 | a0001c0001t0001g0033 | 2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.307+3432C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096433 | ||||||
chr16:9096547
|
G | C | 136 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(133): Show | 210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.307+3546G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096547 | ||||||
chr16:9096556
|
G | A | 134 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(131): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.307+3555G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096556 | ||||||
chr16:9096704
|
C | G | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.307+3703C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096704 | ||||||
chr16:9096729
|
C | T | 135 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(132): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.307+3728C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096729 | ||||||
chr16:9096827
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.307+3826C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096827 | ||||||
chr16:9096892
|
A | T | 169 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(166): Show | 266 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.307+3891A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9096892 | ||||||
chr16:9097033
|
T | C | 1 | a0001c0001t0012g0071 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.307+4032T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097033 | ||||||
chr16:9097073
|
G | T | 2 | a0001c0001t0020g0175a0001c0001t0064g0156 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.307+4072G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097073 | ||||||
chr16:9097187
|
G | A | 1 | a0001c0001t0002g0025 | 3 | NA18961.hp2 NA18965.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.307+4186G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097187 | ||||||
chr16:9097237
|
GCT | G | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+4239_307+4240d others(4): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9097237 | |||||
chr16:9097240
|
C | CT | 165 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0095others(162): Show | 260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.307+4254dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9097240 | |||||
chr16:9097316
|
C | G | 7 | a0002c0002t0016g0009a0002c0002t0016g0023a0002c0002t0016g0152others(4): Show | 12 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.307+4315C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097316 | ||||||
chr16:9097388
|
C | T | 1 | a0001c0005t0044g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.307+4387C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097388 | ||||||
chr16:9097468
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.307+4467C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097468 | ||||||
chr16:9097481
|
C | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0151a0001c0001t0078g0014others(2): Show | 8 | HG01891.hp1 HG02280.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.307+4480C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097481 | ||||||
chr16:9097585
|
AAC | A | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+4588_307+4589d others(4): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9097585 | |||||
chr16:9097669
|
G | A | 3 | a0001c0001t0008g0116a0001c0001t0008g0117a0001c0001t0008g0118 | 3 | NA18939.hp2 NA19078.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.307+4668G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097669 | ||||||
chr16:9097793
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.307+4792G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097793 | ||||||
chr16:9097803
|
A | G | 1 | a0001c0001t0084g0149 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.307+4802A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097803 | ||||||
chr16:9097895
|
G | C | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.307+4894G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097895 | ||||||
chr16:9097933
|
C | T | 52 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(49): Show | 72 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.307+4932C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9097933 | ||||||
chr16:9098105
|
A | T | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0001c0008t0009g0177 | 5 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-4879A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098105 | ||||||
chr16:9098135
|
A | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.308-4849A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098135 | ||||||
chr16:9098173
|
A | C | 34 | a0001c0001t0001g0068a0001c0001t0003g0003a0001c0001t0003g0021others(31): Show | 51 | HG00438.hp2 HG00673.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.308-4811A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098173 | ||||||
chr16:9098256
|
C | G | 1 | a0001c0001t0032g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.308-4728C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098256 | ||||||
chr16:9098259
|
G | C | 1 | a0001c0001t0029g0119 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.308-4725G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098259 | ||||||
chr16:9098354
|
C | T | 1 | a0001c0001t0023g0051 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.308-4630C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098354 | ||||||
chr16:9098423
|
G | A | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.308-4561G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098423 | ||||||
chr16:9098441
|
G | A | 170 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(167): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.308-4543G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098441 | ||||||
chr16:9098621
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.308-4363G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098621 | ||||||
chr16:9098673
|
A | C | 1 | a0001c0001t0032g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.308-4311A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098673 | ||||||
chr16:9098759
|
T | C | 146 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(143): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.308-4225T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098759 | ||||||
chr16:9098800
|
G | A | 25 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(22): Show | 48 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.308-4184G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098800 | ||||||
chr16:9098800
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.308-4184G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098800 | ||||||
chr16:9098950
|
G | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308-4034G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098950 | ||||||
chr16:9098974
|
G | C | 1 | a0001c0001t0032g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.308-4010G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9098974 | ||||||
chr16:9099139
|
AG | A | 134 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(131): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.308-3844delG | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099139 | ||||||
chr16:9099140
|
G | A | 36 | a0001c0001t0001g0068a0001c0001t0003g0003a0001c0001t0003g0021others(33): Show | 53 | HG00438.hp2 HG00673.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.308-3844G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099140 | ||||||
chr16:9099159
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.308-3825G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099159 | ||||||
chr16:9099170
|
A | G | 1 | a0001c0001t0005g0104 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.308-3814A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099170 | ||||||
chr16:9099256
|
G | T | 3 | a0001c0001t0004g0049a0001c0001t0004g0198a0001c0001t0048g0049 | 3 | HG02602.hp1 HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.308-3728G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099256 | ||||||
chr16:9099263
|
TCTTGGCT others(2): Show |
T | 15 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(12): Show | 33 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.308-3720_308-3712d others(11): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099263 | ||||||
chr16:9099273
|
T | G | 15 | a0001c0001t0005g0001a0001c0001t0005g0199a0001c0001t0005g0200others(12): Show | 33 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.308-3711T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099273 | ||||||
chr16:9099316
|
G | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0066a0001c0001t0002g0185others(2): Show | 7 | HG01256.hp1 HG01258.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.308-3668G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099316 | ||||||
chr16:9099316
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.308-3668G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099316 | ||||||
chr16:9099338
|
G | C | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308-3646G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099338 | ||||||
chr16:9099451
|
C | T | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.308-3533C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099451 | ||||||
chr16:9099548
|
T | A | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.308-3436T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099548 | ||||||
chr16:9099585
|
A | C | 148 | a0001c0001t0001g0068a0001c0001t0002g0004a0001c0001t0002g0017others(145): Show | 224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.308-3399A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099585 | ||||||
chr16:9099637
|
C | T | 2 | a0001c0001t0023g0051a0001c0001t0034g0215 | 3 | HG02615.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.308-3347C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099637 | ||||||
chr16:9099866
|
T | G | 56 | a0001c0001t0001g0068a0001c0001t0003g0003a0001c0001t0003g0021others(53): Show | 93 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.308-3118T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099866 | ||||||
chr16:9099887
|
A | C | 1 | a0002c0002t0040g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.308-3097A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9099887 | ||||||
chr16:9100024
|
C | T | 1 | a0001c0001t0005g0203 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.308-2960C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100024 | ||||||
chr16:9100210
|
A | G | 2 | a0001c0001t0023g0051a0001c0001t0034g0215 | 3 | HG02615.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.308-2774A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100210 | ||||||
chr16:9100271
|
C | A | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0002c0002t0040g0123 | 5 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-2713C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100271 | ||||||
chr16:9100366
|
T | C | 1 | a0001c0001t0009g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.308-2618T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100366 | ||||||
chr16:9100417
|
A | AG | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.308-2567_308-2566i others(3): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100417 | ||||||
chr16:9100417
|
AT | A | 6 | a0001c0001t0002g0187a0001c0001t0003g0124a0001c0001t0003g0176others(3): Show | 6 | HG03041.hp1 HG03041.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-2553delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9100417 | |||||
chr16:9100418
|
T | G | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308-2566T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100418 | ||||||
chr16:9100422
|
T | A | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308-2562T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100422 | ||||||
chr16:9100518
|
G | A | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308-2466G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100518 | ||||||
chr16:9100532
|
T | C | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0001c0008t0009g0177 | 5 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-2452T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100532 | ||||||
chr16:9100572
|
C | T | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.308-2412C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100572 | ||||||
chr16:9100597
|
A | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.308-2387A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100597 | ||||||
chr16:9100681
|
C | G | 12 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(9): Show | 16 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-2303C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100681 | ||||||
chr16:9100681
|
C | T | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.308-2303C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100681 | ||||||
chr16:9100806
|
A | AT | 2 | a0001c0001t0020g0043a0001c0001t0065g0180 | 3 | HG02886.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.308-2176dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9100806 | |||||
chr16:9100921
|
G | C | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0001c0008t0009g0177 | 5 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-2063G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100921 | ||||||
chr16:9100939
|
C | G | 1 | a0001c0003t0030g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.308-2045C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100939 | ||||||
chr16:9100965
|
C | T | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0001c0008t0009g0177 | 5 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-2019C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100965 | ||||||
chr16:9100967
|
C | G | 25 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(22): Show | 48 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.308-2017C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9100967 | ||||||
chr16:9101039
|
G | A | 1 | a0001c0001t0010g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.308-1945G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101039 | ||||||
chr16:9101048
|
C | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308-1936C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101048 | ||||||
chr16:9101094
|
G | T | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0002c0002t0040g0123 | 5 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-1890G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101094 | ||||||
chr16:9101106
|
T | C | 111 | a0001c0001t0001g0068a0001c0001t0001g0153a0001c0001t0003g0003others(108): Show | 158 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.308-1878T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101106 | ||||||
chr16:9101193
|
T | C | 147 | a0001c0001t0001g0068a0001c0001t0001g0153a0001c0001t0002g0004others(144): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.308-1791T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101193 | ||||||
chr16:9101238
|
T | C | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.308-1746T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101238 | ||||||
chr16:9101247
|
G | A | 147 | a0001c0001t0001g0068a0001c0001t0001g0153a0001c0001t0002g0004others(144): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.308-1737G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101247 | ||||||
chr16:9101440
|
G | C | 2 | a0001c0001t0023g0051a0001c0001t0034g0215 | 3 | HG02615.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.308-1544G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101440 | ||||||
chr16:9101470
|
C | T | 1 | a0001c0001t0027g0032 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.308-1514C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101470 | ||||||
chr16:9101497
|
T | A | 21 | a0001c0001t0005g0001a0001c0001t0005g0104a0001c0001t0005g0199others(18): Show | 41 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.308-1487T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101497 | ||||||
chr16:9101570
|
T | G | 1 | a0001c0001t0003g0125 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.308-1414T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101570 | ||||||
chr16:9101742
|
AT | A | 144 | a0001c0001t0001g0068a0001c0001t0001g0101a0001c0001t0001g0153others(141): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.308-1226delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 9101742 | |||||
chr16:9101846
|
T | G | 171 | a0001c0001t0001g0068a0001c0001t0001g0153a0001c0001t0002g0004others(168): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.308-1138T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9101846 | ||||||
chr16:9102017
|
A | C | 1 | a0001c0001t0007g0042 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.308-967A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102017 | ||||||
chr16:9102028
|
G | C | 1 | a0001c0001t0032g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.308-956G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102028 | ||||||
chr16:9102094
|
A | G | 1 | a0001c0001t0021g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.308-890A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102094 | ||||||
chr16:9102095
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.308-889G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102095 | ||||||
chr16:9102126
|
C | T | 1 | a0001c0001t0001g0030 | 2 | HG01175.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.308-858C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102126 | ||||||
chr16:9102141
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0022g0028 | 3 | HG02080.hp1 NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.308-843C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102141 | ||||||
chr16:9102142
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.308-842G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102142 | ||||||
chr16:9102301
|
T | TA | 171 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0153others(168): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.308-683_308-682ins others(1): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102301 | ||||||
chr16:9102405
|
T | C | 3 | a0001c0001t0003g0127a0001c0001t0019g0126a0001c0001t0055g0171 | 3 | HG01123.hp1 HG01346.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.308-579T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102405 | ||||||
chr16:9102511
|
A | G | 5 | a0001c0001t0013g0029a0001c0001t0013g0178a0001c0001t0032g0053others(2): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.308-473A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102511 | ||||||
chr16:9102548
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.308-436T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102548 | ||||||
chr16:9102570
|
A | G | 3 | a0001c0001t0013g0029a0001c0001t0013g0178a0001c0001t0032g0053 | 5 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-414A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102570 | ||||||
chr16:9102606
|
C | T | 18 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(15): Show | 26 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.308-378C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102606 | ||||||
chr16:9102714
|
A | G | 1 | a0001c0001t0003g0136 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.308-270A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102714 | ||||||
chr16:9102781
|
A | G | 3 | a0001c0001t0075g0096a0001c0001t0076g0097a0001c0001t0081g0098 | 3 | HG02622.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.308-203A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 2/3 | chr16 | 9102781 | ||||||
chr16:9103416
|
A | T | 3 | a0001c0001t0013g0029a0001c0001t0013g0178a0001c0001t0032g0053 | 5 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.583+157A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103416 | ||||||
chr16:9103502
|
C | T | 1 | a0001c0001t0026g0122 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.583+243C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103502 | ||||||
chr16:9103512
|
T | C | 19 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(16): Show | 26 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.583+253T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103512 | ||||||
chr16:9103513
|
G | A | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.583+254G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103513 | ||||||
chr16:9103572
|
A | G | 2 | a0001c0001t0004g0147a0001c0001t0004g0174 | 2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.583+313A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103572 | ||||||
chr16:9103611
|
T | A | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+352T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103611 | ||||||
chr16:9103746
|
C | T | 1 | a0001c0001t0029g0119 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.583+487C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103746 | ||||||
chr16:9103789
|
A | G | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+530A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103789 | ||||||
chr16:9103806
|
G | C | 1 | a0001c0001t0077g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.583+547G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103806 | ||||||
chr16:9103912
|
A | T | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+653A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103912 | ||||||
chr16:9103994
|
G | T | 7 | a0001c0001t0013g0029a0001c0001t0023g0051a0001c0001t0032g0053others(4): Show | 10 | HG01167.hp1 HG01169.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.583+735G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9103994 | ||||||
chr16:9104020
|
C | CAG | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+763_583+764dup others(2): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9104020 | |||||
chr16:9104114
|
C | CT | 15 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(12): Show | 18 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.583+871dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9104114 | |||||
chr16:9104114
|
C | T | 1 | a0001c0001t0002g0027 | 3 | NA18967.hp1 NA18969.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.583+855C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104114 | ||||||
chr16:9104114
|
CT | C | 65 | a0001c0001t0001g0074a0001c0001t0002g0004a0001c0001t0002g0017others(62): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.583+871delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9104114 | |||||
chr16:9104115
|
T | C | 1 | a0001c0001t0002g0027 | 3 | NA18967.hp1 NA18969.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.583+856T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104115 | ||||||
chr16:9104120
|
T | C | 1 | a0001c0001t0032g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.583+861T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104120 | ||||||
chr16:9104149
|
T | C | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+890T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104149 | ||||||
chr16:9104182
|
T | C | 1 | a0001c0001t0007g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.583+923T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104182 | ||||||
chr16:9104201
|
A | G | 1 | a0001c0001t0009g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.583+942A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104201 | ||||||
chr16:9104278
|
A | G | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+1019A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104278 | ||||||
chr16:9104303
|
G | A | 1 | a0001c0001t0056g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.583+1044G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104303 | ||||||
chr16:9104305
|
G | C | 7 | a0001c0001t0007g0015a0001c0001t0007g0042a0001c0001t0007g0138others(4): Show | 10 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+1046G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104305 | ||||||
chr16:9104394
|
C | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+1135C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104394 | ||||||
chr16:9104435
|
C | T | 1 | a0001c0001t0014g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.583+1176C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104435 | ||||||
chr16:9104710
|
A | G | 2 | a0001c0001t0013g0029a0001c0001t0032g0053 | 4 | HG01167.hp1 HG01169.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+1451A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104710 | ||||||
chr16:9104722
|
T | C | 8 | a0001c0001t0013g0034a0002c0002t0016g0009a0002c0002t0016g0023others(5): Show | 14 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.583+1463T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104722 | ||||||
chr16:9104899
|
A | G | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.583+1640A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104899 | ||||||
chr16:9104928
|
G | C | 3 | a0001c0001t0013g0029a0001c0001t0032g0053a0001c0008t0009g0177 | 5 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.583+1669G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104928 | ||||||
chr16:9104970
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.583+1711A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9104970 | ||||||
chr16:9105005
|
A | G | 1 | a0001c0001t0036g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.583+1746A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105005 | ||||||
chr16:9105052
|
A | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583+1793A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105052 | ||||||
chr16:9105078
|
C | T | 1 | a0001c0001t0004g0174 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.583+1819C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105078 | ||||||
chr16:9105100
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.583+1841A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105100 | ||||||
chr16:9105109
|
A | G | 61 | a0001c0001t0001g0153a0001c0001t0002g0004a0001c0001t0002g0017others(58): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.583+1850A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105109 | ||||||
chr16:9105130
|
G | C | 146 | a0001c0001t0001g0153a0001c0001t0002g0004a0001c0001t0002g0017others(143): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.583+1871G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105130 | ||||||
chr16:9105179
|
T | A | 147 | a0001c0001t0001g0153a0001c0001t0002g0004a0001c0001t0002g0017others(144): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.583+1920T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105179 | ||||||
chr16:9105193
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.583+1934G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105193 | ||||||
chr16:9105275
|
T | G | 2 | a0001c0001t0032g0053a0002c0002t0040g0123 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.583+2016T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105275 | ||||||
chr16:9105356
|
C | G | 20 | a0001c0001t0005g0001a0001c0001t0005g0104a0001c0001t0005g0199others(17): Show | 38 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.583+2097C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105356 | ||||||
chr16:9105447
|
G | C | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+2188G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105447 | ||||||
chr16:9105487
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.583+2228T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105487 | ||||||
chr16:9105524
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.583+2265G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105524 | ||||||
chr16:9105616
|
G | A | 1 | a0001c0001t0001g0048 | 2 | HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.583+2357G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105616 | ||||||
chr16:9105652
|
ATAGT | A | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+2397_583+2400d others(6): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9105652 | |||||
chr16:9105780
|
C | T | 1 | a0001c0001t0083g0192 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.583+2521C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105780 | ||||||
chr16:9105813
|
C | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+2554C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105813 | ||||||
chr16:9105951
|
C | T | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+2692C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105951 | ||||||
chr16:9105995
|
C | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.583+2736C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9105995 | ||||||
chr16:9106163
|
C | T | 1 | a0001c0001t0079g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583+2904C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106163 | ||||||
chr16:9106262
|
A | G | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+3003A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106262 | ||||||
chr16:9106265
|
G | T | 1 | a0001c0005t0044g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583+3006G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106265 | ||||||
chr16:9106292
|
G | GT | 28 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0091others(25): Show | 33 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.583+3050dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9106292 | |||||
chr16:9106292
|
G | T | 1 | a0001c0001t0006g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.583+3033G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106292 | ||||||
chr16:9106343
|
G | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+3084G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106343 | ||||||
chr16:9106346
|
T | C | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+3087T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106346 | ||||||
chr16:9106375
|
GT | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.583+3118delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9106375 | |||||
chr16:9106381
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.583+3122A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106381 | ||||||
chr16:9106382
|
T | G | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+3123T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106382 | ||||||
chr16:9106425
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.583+3166G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106425 | ||||||
chr16:9106432
|
A | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+3173A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106432 | ||||||
chr16:9106437
|
G | A | 13 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0027others(10): Show | 29 | HG00597.hp1 HG00621.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.583+3178G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106437 | ||||||
chr16:9106440
|
C | T | 1 | a0002c0002t0016g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.583+3181C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106440 | ||||||
chr16:9106465
|
A | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(186): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.583+3206A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106465 | ||||||
chr16:9106466
|
G | A | 2 | a0001c0001t0003g0130a0001c0001t0084g0149 | 2 | HG01255.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.583+3207G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106466 | ||||||
chr16:9106504
|
A | T | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+3245A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106504 | ||||||
chr16:9106579
|
C | T | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.583+3320C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106579 | ||||||
chr16:9106690
|
T | C | 56 | a0001c0001t0001g0153a0001c0001t0003g0003a0001c0001t0003g0021others(53): Show | 91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.583+3431T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106690 | ||||||
chr16:9106765
|
T | G | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.583+3506T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106765 | ||||||
chr16:9106850
|
C | T | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.583+3591C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106850 | ||||||
chr16:9106856
|
G | A | 1 | a0001c0001t0015g0077 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.583+3597G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106856 | ||||||
chr16:9106871
|
G | A | 26 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(23): Show | 49 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.583+3612G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106871 | ||||||
chr16:9106938
|
T | A | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583+3679T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9106938 | ||||||
chr16:9107053
|
T | C | 56 | a0001c0001t0001g0153a0001c0001t0003g0003a0001c0001t0003g0021others(53): Show | 91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.583+3794T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107053 | ||||||
chr16:9107101
|
C | G | 16 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0035others(13): Show | 23 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.583+3842C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107101 | ||||||
chr16:9107139
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.583+3880C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107139 | ||||||
chr16:9107260
|
G | A | 1 | a0001c0001t0032g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.583+4001G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107260 | ||||||
chr16:9107334
|
T | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.583+4075T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107334 | ||||||
chr16:9107476
|
C | G | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583+4217C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107476 | ||||||
chr16:9107548
|
G | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0066a0001c0001t0002g0185others(2): Show | 7 | HG01256.hp1 HG01258.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.583+4289G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107548 | ||||||
chr16:9107621
|
G | C | 1 | a0001c0001t0013g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.583+4362G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107621 | ||||||
chr16:9107686
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.583+4427C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107686 | ||||||
chr16:9107911
|
T | C | 1 | a0001c0001t0009g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.583+4652T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107911 | ||||||
chr16:9107914
|
G | A | 1 | a0001c0001t0009g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.583+4655G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107914 | ||||||
chr16:9107945
|
CAG | C | 3 | a0001c0001t0001g0073a0001c0001t0072g0084a0001c0001t0073g0202 | 3 | HG00733.hp2 HG01123.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.583+4689_583+4690d others(4): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9107945 | |||||
chr16:9107988
|
C | T | 1 | a0001c0001t0002g0047 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.583+4729C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9107988 | ||||||
chr16:9108075
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.583+4816C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108075 | ||||||
chr16:9108084
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.583+4825G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108084 | ||||||
chr16:9108113
|
G | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.583+4854G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108113 | ||||||
chr16:9108114
|
G | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+4855G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108114 | ||||||
chr16:9108177
|
G | A | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.583+4918G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108177 | ||||||
chr16:9108244
|
GAT | G | 8 | a0001c0001t0008g0008a0001c0001t0008g0116a0001c0001t0008g0117others(5): Show | 13 | HG01928.hp2 HG02071.hp2 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.583+4988_583+4989d others(4): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9108244 | |||||
chr16:9108250
|
G | C | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583+4991G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108250 | ||||||
chr16:9108384
|
C | G | 27 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(24): Show | 50 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.583+5125C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108384 | ||||||
chr16:9108439
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.583+5180A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108439 | ||||||
chr16:9108440
|
C | A | 4 | a0001c0001t0023g0051a0001c0001t0032g0053a0001c0001t0032g0204others(1): Show | 5 | HG02615.hp2 HG02647.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.583+5181C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108440 | ||||||
chr16:9108460
|
A | G | 2 | a0001c0001t0028g0036a0001c0006t0029g0165 | 3 | HG02055.hp2 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.583+5201A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108460 | ||||||
chr16:9108517
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+5258C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108517 | ||||||
chr16:9108546
|
C | T | 5 | a0001c0001t0003g0045a0001c0001t0014g0022a0001c0001t0014g0133others(2): Show | 7 | HG00438.hp2 NA18940.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.583+5287C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108546 | ||||||
chr16:9108594
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.583+5335G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108594 | ||||||
chr16:9108678
|
G | T | 19 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0035others(16): Show | 26 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.583+5419G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108678 | ||||||
chr16:9108680
|
G | T | 1 | a0001c0001t0058g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.583+5421G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9108680 | ||||||
chr16:9108692
|
T | TA | 1 | a0002c0002t0016g0023 | 3 | HG02630.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.583+5436dupA | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9108692 | |||||
chr16:9109002
|
G | C | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+5743G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109002 | ||||||
chr16:9109094
|
A | G | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+5835A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109094 | ||||||
chr16:9109138
|
A | G | 1 | a0001c0001t0085g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.583+5879A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109138 | ||||||
chr16:9109185
|
G | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+5926G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109185 | ||||||
chr16:9109192
|
G | C | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+5933G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109192 | ||||||
chr16:9109226
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.583+5967C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109226 | ||||||
chr16:9109354
|
G | A | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583+6095G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109354 | ||||||
chr16:9109362
|
T | C | 14 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(11): Show | 19 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.583+6103T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109362 | ||||||
chr16:9109485
|
G | A | 1 | a0001c0001t0064g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.583+6226G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109485 | ||||||
chr16:9109540
|
A | T | 18 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0035others(15): Show | 25 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.583+6281A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109540 | ||||||
chr16:9109737
|
T | A | 153 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(150): Show | 232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.583+6478T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109737 | ||||||
chr16:9109777
|
A | C | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.583+6518A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109777 | ||||||
chr16:9109791
|
A | C | 138 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(135): Show | 212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.583+6532A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109791 | ||||||
chr16:9109792
|
C | CT | 13 | a0001c0001t0013g0034a0001c0001t0013g0178a0001c0001t0028g0036others(10): Show | 20 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.583+6543dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9109792 | |||||
chr16:9109869
|
T | G | 1 | a0001c0001t0008g0120 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.583+6610T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109869 | ||||||
chr16:9109904
|
A | C | 1 | a0001c0001t0011g0190 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.583+6645A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9109904 | ||||||
chr16:9110014
|
A | G | 153 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(150): Show | 232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.584-6654A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110014 | ||||||
chr16:9110042
|
G | A | 18 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(15): Show | 26 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.584-6626G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110042 | ||||||
chr16:9110113
|
A | G | 1 | a0001c0001t0039g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.584-6555A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110113 | ||||||
chr16:9110158
|
C | CT | 76 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0074others(73): Show | 113 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(110): Show |
intron_variant | MODIFIER | c.584-6493dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9110158 | |||||
chr16:9110158
|
C | CTT | 79 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(76): Show | 125 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.584-6494_584-6493d others(4): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9110158 | |||||
chr16:9110158
|
C | CTTT | 5 | a0001c0001t0003g0021a0001c0001t0003g0132a0001c0001t0003g0172others(2): Show | 6 | HG03942.hp1 NA18965.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.584-6495_584-6493d others(5): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9110158 | |||||
chr16:9110158
|
CT | C | 19 | a0001c0001t0001g0093a0001c0001t0005g0001a0001c0001t0005g0104others(16): Show | 37 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.584-6493delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9110158 | |||||
chr16:9110340
|
A | C | 1 | a0001c0008t0009g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.584-6328A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110340 | ||||||
chr16:9110355
|
G | T | 3 | a0001c0001t0032g0053a0001c0001t0032g0204a0002c0002t0040g0123 | 3 | HG03486.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-6313G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110355 | ||||||
chr16:9110641
|
C | T | 2 | a0001c0001t0060g0031a0001c0001t0061g0031 | 2 | NA18977.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.584-6027C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110641 | ||||||
chr16:9110656
|
C | T | 1 | a0001c0001t0009g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.584-6012C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110656 | ||||||
chr16:9110671
|
T | A | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.584-5997T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110671 | ||||||
chr16:9110700
|
C | T | 1 | a0001c0001t0003g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.584-5968C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110700 | ||||||
chr16:9110716
|
A | G | 16 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(13): Show | 21 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.584-5952A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110716 | ||||||
chr16:9110854
|
T | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-5814T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110854 | ||||||
chr16:9110898
|
G | A | 1 | a0001c0001t0011g0188 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.584-5770G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110898 | ||||||
chr16:9110905
|
G | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-5763G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110905 | ||||||
chr16:9110948
|
G | T | 48 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(45): Show | 69 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.584-5720G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110948 | ||||||
chr16:9110953
|
G | T | 2 | a0001c0001t0020g0043a0001c0001t0065g0180 | 3 | HG02886.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.584-5715G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110953 | ||||||
chr16:9110978
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.584-5690C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110978 | ||||||
chr16:9110986
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.584-5682T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9110986 | ||||||
chr16:9111036
|
C | A | 1 | a0001c0001t0006g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.584-5632C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111036 | ||||||
chr16:9111050
|
C | CA | 173 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(170): Show | 270 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.584-5613dupA | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9111050 | |||||
chr16:9111158
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0021g0092 | 2 | NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.584-5510T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111158 | ||||||
chr16:9111299
|
G | C | 1 | a0001c0001t0006g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.584-5369G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111299 | ||||||
chr16:9111452
|
A | G | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-5216A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111452 | ||||||
chr16:9111506
|
T | C | 49 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(46): Show | 70 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.584-5162T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111506 | ||||||
chr16:9111519
|
T | G | 2 | a0001c0001t0003g0046a0001c0001t0003g0176 | 3 | NA18984.hp2 NA19054.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.584-5149T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111519 | ||||||
chr16:9111554
|
A | G | 2 | a0001c0005t0044g0214a0001c0008t0009g0177 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.584-5114A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111554 | ||||||
chr16:9111629
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-5039C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111629 | ||||||
chr16:9111815
|
T | G | 3 | a0001c0001t0032g0053a0001c0001t0032g0204a0002c0002t0040g0123 | 3 | HG03486.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-4853T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9111815 | ||||||
chr16:9111907
|
AT | A | 173 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(170): Show | 270 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.584-4759delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9111907 | |||||
chr16:9112125
|
C | G | 16 | a0001c0001t0005g0001a0001c0001t0005g0104a0001c0001t0005g0199others(13): Show | 34 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.584-4543C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112125 | ||||||
chr16:9112132
|
A | C | 1 | a0001c0001t0005g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.584-4536A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112132 | ||||||
chr16:9112551
|
C | T | 1 | a0001c0001t0001g0030 | 2 | HG01175.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.584-4117C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112551 | ||||||
chr16:9112686
|
G | C | 1 | a0001c0001t0035g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.584-3982G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112686 | ||||||
chr16:9112694
|
A | G | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.584-3974A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112694 | ||||||
chr16:9112715
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.584-3953A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112715 | ||||||
chr16:9112737
|
C | G | 2 | a0001c0001t0006g0016a0001c0001t0006g0169 | 5 | HG01884.hp1 HG02486.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.584-3931C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112737 | ||||||
chr16:9112775
|
C | G | 1 | a0001c0001t0020g0175 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.584-3893C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112775 | ||||||
chr16:9112800
|
C | A | 1 | a0001c0004t0001g0086 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.584-3868C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112800 | ||||||
chr16:9112823
|
A | G | 1 | a0001c0001t0008g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.584-3845A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112823 | ||||||
chr16:9112940
|
T | C | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-3728T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9112940 | ||||||
chr16:9113005
|
G | GT | 12 | a0001c0001t0003g0124a0001c0001t0009g0012a0001c0001t0009g0158others(9): Show | 17 | HG01243.hp2 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.584-3651dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9113005 | |||||
chr16:9113005
|
G | T | 1 | a0001c0001t0064g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.584-3663G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113005 | ||||||
chr16:9113005
|
GT | G | 99 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(96): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.584-3651delT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9113005 | |||||
chr16:9113017
|
T | G | 1 | a0001c0001t0057g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.584-3651T>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113017 | ||||||
chr16:9113018
|
G | T | 5 | a0001c0001t0005g0200a0001c0001t0032g0053a0001c0001t0032g0204others(2): Show | 5 | HG01978.hp2 HG02071.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.584-3650G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113018 | ||||||
chr16:9113037
|
G | GT | 7 | a0001c0001t0001g0019a0001c0001t0002g0195a0001c0001t0006g0151others(4): Show | 11 | HG01346.hp1 HG01358.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.584-3621dupT | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9113037 | |||||
chr16:9113037
|
G | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-3631G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113037 | ||||||
chr16:9113146
|
T | C | 91 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(88): Show | 129 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(126): Show |
intron_variant | MODIFIER | c.584-3522T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113146 | ||||||
chr16:9113179
|
G | A | 1 | a0001c0001t0063g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.584-3489G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113179 | ||||||
chr16:9113215
|
C | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-3453C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113215 | ||||||
chr16:9113342
|
C | A | 61 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0049others(58): Show | 88 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.584-3326C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113342 | ||||||
chr16:9113600
|
T | C | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.584-3068T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113600 | ||||||
chr16:9113672
|
A | T | 172 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(169): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.584-2996A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113672 | ||||||
chr16:9113704
|
G | A | 1 | a0001c0001t0018g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.584-2964G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113704 | ||||||
chr16:9113786
|
C | G | 15 | a0001c0001t0009g0012a0001c0001t0009g0158a0001c0001t0009g0161others(12): Show | 20 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.584-2882C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113786 | ||||||
chr16:9113803
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-2865C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113803 | ||||||
chr16:9113883
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-2785C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113883 | ||||||
chr16:9113896
|
T | C | 172 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(169): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.584-2772T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113896 | ||||||
chr16:9113959
|
T | C | 35 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0037others(32): Show | 52 | HG00438.hp2 HG00673.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.584-2709T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113959 | ||||||
chr16:9113964
|
G | A | 1 | a0002c0002t0016g0023 | 3 | HG02630.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.584-2704G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9113964 | ||||||
chr16:9114001
|
G | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-2667G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114001 | ||||||
chr16:9114135
|
G | C | 1 | a0001c0001t0005g0199 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.584-2533G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114135 | ||||||
chr16:9114471
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-2197C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114471 | ||||||
chr16:9114581
|
C | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(248): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.584-2087C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114581 | ||||||
chr16:9114582
|
G | C | 17 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0035others(14): Show | 24 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.584-2086G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114582 | ||||||
chr16:9114639
|
C | G | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-2029C>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114639 | ||||||
chr16:9114687
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.584-1981G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114687 | ||||||
chr16:9114705
|
T | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1963T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114705 | ||||||
chr16:9114770
|
G | C | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1898G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114770 | ||||||
chr16:9114799
|
T | C | 1 | a0001c0001t0013g0029 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.584-1869T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114799 | ||||||
chr16:9114848
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.584-1820T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114848 | ||||||
chr16:9114868
|
A | G | 1 | a0001c0001t0008g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.584-1800A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114868 | ||||||
chr16:9114931
|
C | A | 1 | a0001c0001t0034g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.584-1737C>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114931 | ||||||
chr16:9114956
|
G | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1712G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114956 | ||||||
chr16:9114977
|
C | T | 1 | a0001c0001t0003g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.584-1691C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114977 | ||||||
chr16:9114991
|
A | G | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1677A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114991 | ||||||
chr16:9114995
|
G | A | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1673G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9114995 | ||||||
chr16:9115017
|
G | A | 1 | a0001c0001t0013g0034 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.584-1651G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115017 | ||||||
chr16:9115265
|
T | A | 170 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(167): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.584-1403T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115265 | ||||||
chr16:9115278
|
A | C | 3 | a0001c0001t0007g0042a0001c0001t0007g0139a0001c0001t0007g0140 | 4 | HG02895.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-1390A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115278 | ||||||
chr16:9115337
|
T | C | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1331T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115337 | ||||||
chr16:9115450
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.584-1218A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115450 | ||||||
chr16:9115474
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.584-1194G>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115474 | ||||||
chr16:9115499
|
T | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0068others(10): Show | 15 | HG00597.hp2 HG00621.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.584-1169T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115499 | ||||||
chr16:9115652
|
C | T | 3 | a0001c0001t0032g0053a0001c0001t0032g0204a0002c0002t0040g0123 | 3 | HG03486.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-1016C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115652 | ||||||
chr16:9115699
|
CCGCCTCC others(6): Show |
C | 1 | a0001c0001t0003g0038 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.584-967_584-955del others(13): Show |
HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 9115699 | |||||
chr16:9115700
|
C | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-968C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115700 | ||||||
chr16:9115717
|
C | T | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.584-951C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115717 | ||||||
chr16:9115718
|
G | T | 2 | a0001c0001t0032g0053a0001c0001t0032g0204 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-950G>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115718 | ||||||
chr16:9115739
|
G | A | 1 | a0001c0001t0023g0051 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.584-929G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115739 | ||||||
chr16:9115861
|
C | T | 10 | a0001c0001t0008g0008a0001c0001t0008g0116a0001c0001t0008g0117others(7): Show | 15 | HG01928.hp2 HG02071.hp2 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.584-807C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115861 | ||||||
chr16:9115886
|
A | C | 4 | a0001c0003t0001g0050a0001c0003t0001g0213a0001c0003t0030g0050others(1): Show | 4 | NA18945.hp2 NA18946.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-782A>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9115886 | ||||||
chr16:9116073
|
T | C | 61 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(58): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.584-595T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116073 | ||||||
chr16:9116119
|
T | A | 3 | a0001c0001t0032g0053a0001c0001t0032g0204a0002c0002t0040g0123 | 3 | HG03486.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.584-549T>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116119 | ||||||
chr16:9116124
|
G | A | 3 | a0001c0001t0002g0026a0001c0001t0002g0194a0001c0001t0022g0026 | 4 | HG00140.hp1 HG00323.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-544G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116124 | ||||||
chr16:9116217
|
C | T | 27 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(24): Show | 50 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.584-451C>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116217 | ||||||
chr16:9116241
|
T | C | 19 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0035others(16): Show | 27 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.584-427T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116241 | ||||||
chr16:9116436
|
T | C | 16 | a0001c0001t0006g0014a0001c0001t0006g0016a0001c0001t0006g0035others(13): Show | 23 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.584-232T>C | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116436 | ||||||
chr16:9116449
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.584-219G>A | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116449 | ||||||
chr16:9116516
|
A | T | 146 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0037others(143): Show | 220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.584-152A>T | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116516 | ||||||
chr16:9116533
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.584-135A>G | HAPSTR1 | ENSG00000182831.12 | transcript | ENST00000327827.12 | protein_coding | 3/3 | chr16 | 9116533 |