geneid | 10598 |
---|---|
ensemblid | ENSG00000100591.8 |
hgncid | 1189 |
symbol | AHSA1 |
name | activator of HSP90 ATPase activity 1 |
refseq_nuc | NM_012111.3 |
refseq_prot | NP_036243.1 |
ensembl_nuc | ENST00000216479.8 |
ensembl_prot | ENSP00000216479.3 |
mane_status | MANE Select |
chr | chr14 |
start | 77458093 |
end | 77469472 |
strand | + |
ver | v1.2 |
region | chr14:77458093-77469472 |
region5000 | chr14:77453093-77474472 |
regionname0 | AHSA1_chr14_77458093_77469472 |
regionname5000 | AHSA1_chr14_77453093_77474472 |
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 | 338 | 308 | 94 | 66 | 92 | 14 | 40 | 66 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1017 | 131 | 8 | 26 | 78 | 3 | 15 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0002 | 1/0 | 1017 | 130 | 58 | 28 | 14 | 8 | 21 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0003 | 0/0 | 1017 | 30 | 15 | 8 | 0 | 3 | 4 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0004 | 0/0 | 1017 | 10 | 9 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0005 | 0/0 | 1017 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0006 | 0/0 | 1017 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0007 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0008 | 0/0 | 1017 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
c0009 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 321 | 264 | 81 | 56 | 85 | 11 | 29 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
t0002 | 0/0 | 321 | 32 | 9 | 6 | 6 | 2 | 9 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
t0003 | 0/0 | 321 | 10 | 4 | 4 | 0 | 1 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
t0004 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
t0005 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
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 | 57 | 2 | 15 | 29 | 3 | 8 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0002 | 0/0 | 16 | 4 | 5 | 0 | 0 | 7 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0003 | 1/0 | 14 | 13 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0005 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0006 | 0/0 | 7 | 4 | 2 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0008 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0009 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0011 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0015 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0018 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0019 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1017 | 131 | 8 | 26 | 78 | 3 | 15 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0002 | 1/0 | 1017 | 130 | 58 | 28 | 14 | 8 | 21 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0003 | 0/0 | 1017 | 30 | 15 | 8 | 0 | 3 | 4 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0004 | 0/0 | 1017 | 10 | 9 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0005 | 0/0 | 1017 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0006 | 0/0 | 1017 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0007 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0008 | 0/0 | 1017 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0009 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1337 | 129 | 8 | 26 | 77 | 3 | 14 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0001t0004 | 0/0 | 1337 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0001t0005 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0002t0001 | 1/0 | 1337 | 98 | 49 | 22 | 8 | 6 | 12 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0002t0002 | 0/0 | 1337 | 32 | 9 | 6 | 6 | 2 | 9 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0003t0001 | 0/0 | 1337 | 20 | 11 | 4 | 0 | 2 | 3 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0003t0003 | 0/0 | 1337 | 10 | 4 | 4 | 0 | 1 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0004t0001 | 0/0 | 1337 | 10 | 9 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0005t0001 | 0/0 | 1337 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0006t0001 | 0/0 | 1337 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0007t0001 | 0/0 | 1337 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0008t0001 | 0/0 | 1337 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
a0001c0009t0001 | 0/0 | 1337 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | copy fasta | chr14 | 77453093 | 77474472 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 56 | 2 | 15 | 28 | 3 | 8 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0005 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0015 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0002 | 0/0 | 16 | 4 | 5 | 0 | 0 | 7 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0003 | 1/0 | 14 | 13 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0008 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0011 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0019 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0009 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0003g0006 | 0/0 | 7 | 4 | 2 | 0 | 1 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0004t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0004t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0006t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0008t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
a0001c0009t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0009 | EUR | GBR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0032 | EUR | GBR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0043 | EUR | FIN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00642 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00735 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0046 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01109 | hp2 | a0001 | c0003 | t0003 | g0127 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01243 | hp1 | a0001 | c0004 | t0001 | g0149 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01256 | hp2 | a0001 | c0006 | t0001 | g0023 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01258 | hp2 | a0001 | c0006 | t0001 | g0023 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0009 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0018 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0115 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0025 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0018 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0018 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0112 | EUR | IBS | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01934 | hp2 | a0001 | c0008 | t0001 | g0090 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0128 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0150 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02293 | hp1 | a0001 | c0003 | t0003 | g0126 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02698 | hp2 | a0001 | c0003 | t0003 | g0129 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02717 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0097 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0111 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03130 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0086 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0045 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0106 | AFR | ESN | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03540 | hp2 | a0001 | c0009 | t0001 | g0081 | AFR | GWD | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0119 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0044 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0009 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | BEB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0124 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18522 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | YRI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ASW | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ASW | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0139 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20805 | hp1 | a0001 | c0003 | t0003 | g0006 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0064 | SAS | GIH | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02109 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | MSL | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | USA | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0103 | AFR | LWK | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0051 | REF | REF | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0003 | REF | REF | AHSA1_chr14_77453093_77474472 | AHSA1 | chr14 | 77453093 | 77474472 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77459668
|
C | T | 2 | a0001c0001a0001c0006 | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
synonymous_variant | LOW | c.133C>T | p.Leu45Leu | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/9 | 230/1337 | 133/1017 | 45/338 | chr14 | 77459668 | ||
chr14:77459712
|
G | A | 1 | a0001c0007 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.177G>A | p.Thr59Thr | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/9 | 274/1337 | 177/1017 | 59/338 | chr14 | 77459712 | ||
chr14:77462182
|
A | G | 6 | a0001c0001a0001c0003a0001c0004others(3): Show | 175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
synonymous_variant | LOW | c.294A>G | p.Gln98Gln | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/9 | 391/1337 | 294/1017 | 98/338 | chr14 | 77462182 | ||
chr14:77462203
|
C | T | 2 | a0001c0004a0001c0009 | 11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
synonymous_variant | LOW | c.315C>T | p.Ile105Ile | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/9 | 412/1337 | 315/1017 | 105/338 | chr14 | 77462203 | ||
chr14:77468088
|
G | A | 3 | a0001c0004a0001c0005a0001c0007 | 13 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
synonymous_variant | LOW | c.696G>A | p.Val232Val | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/9 | 793/1337 | 696/1017 | 232/338 | chr14 | 77468088 | ||
chr14:77469177
|
G | A | 3 | a0001c0001a0001c0008a0001c0009 | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
synonymous_variant | LOW | c.945G>A | p.Thr315Thr | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 9/9 | 1042/1337 | 945/1017 | 315/338 | chr14 | 77469177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77458146
|
G | T | 1 | a0001c0001t0005 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/9 | 44 | chr14 | 77458146 | |||||
chr14:77458150
|
C | A | 1 | a0001c0001t0004 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/9 | 40 | chr14 | 77458150 | |||||
chr14:77469316
|
G | A | 1 | a0001c0002t0002 | 32 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*67G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 9/9 | 67 | chr14 | 77469316 | |||||
chr14:77469334
|
G | A | 1 | a0001c0003t0003 | 10 | HG00642.hp2 HG00735.hp2 HG01109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 9/9 | 85 | chr14 | 77469334 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77458390
|
T | G | 1 | a0001c0002t0001g0032 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.80+121T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458390 | ||||||
chr14:77458567
|
T | C | 11 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0033others(8): Show | 13 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+298T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458567 | ||||||
chr14:77458663
|
A | G | 1 | a0001c0002t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.80+394A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458663 | ||||||
chr14:77458811
|
T | C | 1 | a0001c0002t0001g0021 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+542T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77458811 | ||||||
chr14:77458854
|
T | TA | 6 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(3): Show | 7 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+589dupA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 77458854 | |||||
chr14:77459140
|
C | G | 4 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(1): Show | 10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-476C>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459140 | ||||||
chr14:77459181
|
A | G | 6 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(3): Show | 7 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.81-435A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459181 | ||||||
chr14:77459337
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81-279G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459337 | ||||||
chr14:77459342
|
A | G | 11 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0033others(8): Show | 13 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.81-274A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459342 | ||||||
chr14:77459353
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.81-263C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459353 | ||||||
chr14:77459401
|
A | G | 6 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(3): Show | 7 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.81-215A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459401 | ||||||
chr14:77459442
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.81-174C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459442 | ||||||
chr14:77459462
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.81-154A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459462 | ||||||
chr14:77459540
|
A | T | 1 | a0001c0002t0002g0145 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81-76A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 1/8 | chr14 | 77459540 | ||||||
chr14:77460055
|
C | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.271+249C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460055 | ||||||
chr14:77460219
|
G | C | 5 | a0001c0003t0001g0009a0001c0003t0001g0043a0001c0003t0001g0044others(2): Show | 9 | HG00099.hp1 HG00323.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.271+413G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460219 | ||||||
chr14:77460306
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.271+500G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460306 | ||||||
chr14:77460390
|
T | C | 1 | a0001c0001t0001g0013 | 3 | HG00597.hp2 HG01981.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.271+584T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460390 | ||||||
chr14:77460457
|
T | TAAAGAAG others(316): Show |
1 | a0001c0002t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.271+664_271+665ins others(323): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(317): Show |
5 | a0001c0002t0002g0105a0001c0002t0002g0106a0001c0002t0002g0107others(2): Show | 5 | HG01975.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.271+664_271+665ins others(324): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(318): Show |
3 | a0001c0002t0002g0028a0001c0002t0002g0103a0001c0002t0002g0104 | 4 | HG01081.hp1 HG01358.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+664_271+665ins others(325): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(303): Show |
1 | a0001c0007t0001g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+663_271+664ins others(310): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(302): Show |
3 | a0001c0003t0001g0046a0001c0003t0001g0137a0001c0003t0001g0138 | 3 | HG01070.hp1 HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.271+663_271+664ins others(309): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(303): Show |
17 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0003t0001g0009others(14): Show | 28 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(310): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(304): Show |
1 | a0001c0003t0001g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.271+663_271+664ins others(311): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(307): Show |
1 | a0001c0002t0002g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.271+663_271+664ins others(314): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(316): Show |
4 | a0001c0002t0002g0011a0001c0002t0002g0029a0001c0002t0002g0122others(1): Show | 8 | HG02155.hp2 HG02976.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(323): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(317): Show |
6 | a0001c0002t0002g0117a0001c0002t0002g0118a0001c0002t0002g0119others(3): Show | 6 | HG01175.hp2 HG02486.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(324): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(318): Show |
2 | a0001c0002t0002g0019a0001c0002t0002g0116 | 4 | HG01168.hp2 HG02074.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+663_271+664ins others(325): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(319): Show |
3 | a0001c0002t0002g0113a0001c0002t0002g0114a0001c0002t0002g0115 | 3 | HG01099.hp2 HG01515.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.271+663_271+664ins others(326): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460457
|
T | TAAAGAAG others(320): Show |
1 | a0001c0002t0002g0112 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.271+663_271+664ins others(327): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460457 | |||||
chr14:77460572
|
CT | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.271+779delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460572 | |||||
chr14:77460675
|
C | A | 1 | a0001c0009t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.271+869C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460675 | ||||||
chr14:77460710
|
C | A | 2 | a0001c0002t0001g0082a0001c0002t0002g0103 | 2 | HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.271+904C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460710 | ||||||
chr14:77460718
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.271+912C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460718 | ||||||
chr14:77460798
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271+992G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460798 | ||||||
chr14:77460829
|
T | C | 1 | a0001c0002t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271+1023T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460829 | ||||||
chr14:77460887
|
T | C | 1 | a0001c0007t0001g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271+1081T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460887 | ||||||
chr14:77460895
|
A | C | 28 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0002t0001g0132others(25): Show | 41 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.271+1089A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460895 | ||||||
chr14:77460941
|
C | T | 2 | a0001c0003t0001g0135a0001c0003t0001g0136 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.271+1135C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460941 | ||||||
chr14:77460942
|
G | C | 1 | a0001c0002t0001g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.271+1136G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460942 | ||||||
chr14:77460956
|
A | G | 15 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(12): Show | 36 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.271+1150A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460956 | ||||||
chr14:77460971
|
G | A | 25 | a0001c0001t0001g0047a0001c0002t0001g0002a0001c0002t0001g0017others(22): Show | 52 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.271+1165G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460971 | ||||||
chr14:77460976
|
A | G | 15 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(12): Show | 36 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.271+1170A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460976 | ||||||
chr14:77460986
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0079 | 12 | HG02015.hp2 HG02523.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-1174C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460986 | ||||||
chr14:77460987
|
G | A | 16 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(13): Show | 37 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.272-1173G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77460987 | ||||||
chr14:77460994
|
C | CTTT | 16 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(13): Show | 37 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.272-1165_272-1164i others(5): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77460994 | |||||
chr14:77461016
|
C | G | 12 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0033others(9): Show | 14 | HG01109.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.272-1144C>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461016 | ||||||
chr14:77461016
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.272-1144C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461016 | ||||||
chr14:77461017
|
G | A | 1 | a0001c0002t0002g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.272-1143G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461017 | ||||||
chr14:77461020
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.272-1140G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461020 | ||||||
chr14:77461028
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-1132A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461028 | ||||||
chr14:77461029
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-1131T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461029 | ||||||
chr14:77461031
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-1129T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461031 | ||||||
chr14:77461039
|
G | A | 1 | a0001c0002t0001g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.272-1121G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461039 | ||||||
chr14:77461042
|
C | T | 2 | a0001c0005t0001g0086a0001c0005t0001g0097 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.272-1118C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461042 | ||||||
chr14:77461052
|
G | C | 48 | a0001c0002t0001g0088a0001c0002t0001g0132a0001c0002t0001g0133others(45): Show | 67 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.272-1108G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461052 | ||||||
chr14:77461085
|
G | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG01106.hp1 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.272-1075G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461085 | ||||||
chr14:77461109
|
G | T | 14 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(11): Show | 35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.272-1051G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461109 | ||||||
chr14:77461256
|
C | T | 5 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-904C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461256 | ||||||
chr14:77461268
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.272-892C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461268 | ||||||
chr14:77461400
|
C | T | 30 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0026others(27): Show | 46 | HG00099.hp2 HG00741.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-760C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461400 | ||||||
chr14:77461496
|
A | C | 1 | a0001c0004t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.272-664A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461496 | ||||||
chr14:77461520
|
ACT | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0079 | 12 | HG02015.hp2 NA18947.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-637_272-636del others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 77461520 | |||||
chr14:77461531
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.272-629C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461531 | ||||||
chr14:77461549
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.272-611A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461549 | ||||||
chr14:77461627
|
C | A | 8 | a0001c0002t0001g0031a0001c0002t0001g0089a0001c0002t0001g0099others(5): Show | 10 | HG01081.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.272-533C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461627 | ||||||
chr14:77461728
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.272-432G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461728 | ||||||
chr14:77461737
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0032others(2): Show | 13 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.272-423C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461737 | ||||||
chr14:77461940
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.272-220T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461940 | ||||||
chr14:77461945
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 151 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.272-215T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461945 | ||||||
chr14:77461973
|
C | T | 13 | a0001c0003t0001g0009a0001c0003t0001g0030a0001c0003t0001g0043others(10): Show | 25 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.272-187C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77461973 | ||||||
chr14:77462018
|
C | T | 1 | a0001c0002t0001g0143 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.272-142C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77462018 | ||||||
chr14:77462133
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 143 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.272-27C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 2/8 | chr14 | 77462133 | ||||||
chr14:77462254
|
A | C | 1 | a0001c0002t0001g0018 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.354+12A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462254 | ||||||
chr14:77462283
|
T | G | 4 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(1): Show | 10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+41T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462283 | ||||||
chr14:77462294
|
G | C | 1 | a0001c0005t0001g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.354+52G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462294 | ||||||
chr14:77462392
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.354+150A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462392 | ||||||
chr14:77462524
|
G | A | 5 | a0001c0001t0001g0049a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02083.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-118G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462524 | ||||||
chr14:77462560
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.355-82T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 3/8 | chr14 | 77462560 | ||||||
chr14:77462792
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.472+33A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77462792 | ||||||
chr14:77462826
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18939.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.472+67C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77462826 | ||||||
chr14:77462985
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 221 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.472+226A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77462985 | ||||||
chr14:77463008
|
G | A | 2 | a0001c0002t0001g0038a0001c0002t0001g0039 | 2 | HG01109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.472+249G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463008 | ||||||
chr14:77463109
|
G | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.472+350G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463109 | ||||||
chr14:77463323
|
TCA | T | 5 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+568_472+569del others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463323 | |||||
chr14:77463327
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.472+568A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463327 | ||||||
chr14:77463345
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.472+586T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463345 | ||||||
chr14:77463386
|
C | T | 1 | a0001c0003t0003g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472+627C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463386 | ||||||
chr14:77463540
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.472+781C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463540 | ||||||
chr14:77463585
|
C | CA | 8 | a0001c0002t0001g0035a0001c0002t0001g0038a0001c0002t0001g0039others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+840dupA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463585 | |||||
chr14:77463585
|
C | CAA | 19 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(16): Show | 46 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.472+839_472+840dup others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463585 | |||||
chr14:77463585
|
CA | C | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.472+840delA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463585 | |||||
chr14:77463595
|
AAAAAC | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 128 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.472+841_472+845del others(5): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 77463595 | |||||
chr14:77463600
|
C | A | 14 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(11): Show | 16 | HG01081.hp1 HG01109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+841C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463600 | ||||||
chr14:77463648
|
C | T | 5 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(2): Show | 11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.472+889C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463648 | ||||||
chr14:77463708
|
T | C | 1 | a0001c0002t0001g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.473-890T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463708 | ||||||
chr14:77463803
|
G | A | 2 | a0001c0002t0002g0104a0001c0002t0002g0108 | 2 | HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.473-795G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463803 | ||||||
chr14:77463845
|
G | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.473-753G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463845 | ||||||
chr14:77463950
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.473-648C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463950 | ||||||
chr14:77463969
|
T | G | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.473-629T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463969 | ||||||
chr14:77463999
|
G | A | 1 | a0001c0001t0001g0051 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.473-599G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77463999 | ||||||
chr14:77464012
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.473-586T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464012 | ||||||
chr14:77464064
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.473-534G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464064 | ||||||
chr14:77464188
|
C | G | 12 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(9): Show | 18 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.473-410C>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464188 | ||||||
chr14:77464222
|
C | T | 14 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(11): Show | 35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-376C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464222 | ||||||
chr14:77464249
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 168 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.473-349C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464249 | ||||||
chr14:77464334
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.473-264G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464334 | ||||||
chr14:77464369
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.473-229A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464369 | ||||||
chr14:77464381
|
A | T | 4 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(1): Show | 10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.473-217A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464381 | ||||||
chr14:77464409
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 220 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.473-189G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464409 | ||||||
chr14:77464512
|
A | T | 14 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(11): Show | 35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-86A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464512 | ||||||
chr14:77464518
|
G | C | 1 | a0001c0009t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.473-80G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464518 | ||||||
chr14:77464535
|
A | G | 15 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(12): Show | 24 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.473-63A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464535 | ||||||
chr14:77464545
|
A | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0065a0001c0001t0001g0072 | 3 | HG00621.hp1 HG02135.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.473-53A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464545 | ||||||
chr14:77464549
|
C | A | 7 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(4): Show | 8 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-49C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 4/8 | chr14 | 77464549 | ||||||
chr14:77464722
|
A | G | 1 | a0001c0001t0004g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.561+36A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464722 | ||||||
chr14:77464739
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.561+53G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464739 | ||||||
chr14:77464880
|
C | T | 25 | a0001c0002t0002g0011a0001c0002t0002g0019a0001c0002t0002g0028others(22): Show | 32 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.561+194C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464880 | ||||||
chr14:77464888
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.561+202T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464888 | ||||||
chr14:77464910
|
A | T | 7 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+224A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77464910 | ||||||
chr14:77464949
|
A | AG | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.561+264dupG | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 77464949 | |||||
chr14:77465057
|
G | A | 1 | a0001c0009t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.561+371G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465057 | ||||||
chr14:77465158
|
G | T | 4 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(1): Show | 10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-381G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465158 | ||||||
chr14:77465262
|
G | C | 22 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0003t0001g0009others(19): Show | 34 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.562-277G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465262 | ||||||
chr14:77465320
|
T | G | 2 | a0001c0002t0001g0099a0001c0002t0001g0110 | 2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.562-219T>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465320 | ||||||
chr14:77465408
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.562-131A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465408 | ||||||
chr14:77465482
|
G | A | 2 | a0001c0002t0001g0036a0001c0002t0001g0037 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.562-57G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 5/8 | chr14 | 77465482 | ||||||
chr14:77465674
|
A | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
splice_region_variant&intron_variant | LOW | c.690+7A>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465674 | ||||||
chr14:77465734
|
A | G | 5 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+67A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465734 | ||||||
chr14:77465768
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 136 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.690+101A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465768 | ||||||
chr14:77465827
|
C | CT | 8 | a0001c0002t0002g0121a0001c0002t0002g0123a0001c0003t0003g0129others(5): Show | 14 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.690+173dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77465827 | |||||
chr14:77465853
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.690+186C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465853 | ||||||
chr14:77465947
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.690+280G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77465947 | ||||||
chr14:77466137
|
A | G | 3 | a0001c0002t0001g0021a0001c0002t0001g0082a0001c0002t0001g0102 | 4 | HG02258.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+470A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466137 | ||||||
chr14:77466266
|
G | A | 2 | a0001c0002t0002g0105a0001c0002t0002g0106 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.690+599G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466266 | ||||||
chr14:77466276
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 220 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.690+609C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466276 | ||||||
chr14:77466438
|
C | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+771C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466438 | ||||||
chr14:77466439
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0147 | 3 | HG01070.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.690+772G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466439 | ||||||
chr14:77466480
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 220 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.690+813T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466480 | ||||||
chr14:77466623
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.690+956G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466623 | ||||||
chr14:77466624
|
A | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+957A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466624 | ||||||
chr14:77466798
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+1131G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466798 | ||||||
chr14:77466819
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.690+1152G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466819 | ||||||
chr14:77466959
|
G | A | 5 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(2): Show | 11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-1124G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77466959 | ||||||
chr14:77467108
|
T | C | 25 | a0001c0002t0002g0011a0001c0002t0002g0019a0001c0002t0002g0028others(22): Show | 32 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.691-975T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467108 | ||||||
chr14:77467146
|
C | T | 8 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0003t0001g0130others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-937C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467146 | ||||||
chr14:77467163
|
C | A | 1 | a0001c0002t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.691-920C>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467163 | ||||||
chr14:77467265
|
G | A | 1 | a0001c0003t0003g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.691-818G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467265 | ||||||
chr14:77467271
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.691-812C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467271 | ||||||
chr14:77467376
|
G | A | 1 | a0001c0002t0002g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.691-707G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467376 | ||||||
chr14:77467457
|
G | T | 1 | a0001c0002t0002g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.691-626G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467457 | ||||||
chr14:77467552
|
G | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.691-531G>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467552 | ||||||
chr14:77467567
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.691-516G>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467567 | ||||||
chr14:77467627
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.691-456G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467627 | ||||||
chr14:77467643
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.691-440G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467643 | ||||||
chr14:77467650
|
C | T | 7 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(4): Show | 8 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-433C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467650 | ||||||
chr14:77467689
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-394G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467689 | ||||||
chr14:77467700
|
T | A | 10 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(7): Show | 11 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-383T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467700 | ||||||
chr14:77467703
|
A | AT | 10 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0034others(7): Show | 11 | HG02451.hp2 HG02572.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-380_691-379ins others(1): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467703 | ||||||
chr14:77467703
|
AAAAAT | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.691-365_691-361del others(5): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77467703 | |||||
chr14:77467816
|
A | T | 1 | a0001c0003t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.691-267A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467816 | ||||||
chr14:77467938
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.691-145G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467938 | ||||||
chr14:77467950
|
A | G | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02922.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-133A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77467950 | ||||||
chr14:77468049
|
C | CT | 9 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 16 | HG00621.hp2 HG00673.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.691-33dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468049 | |||||
chr14:77468050
|
TC | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0009t0001g0081 | 3 | HG01070.hp2 HG03540.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.691-32delC | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77468050 | ||||||
chr14:77468051
|
C | CT | 41 | a0001c0002t0001g0021a0001c0002t0001g0039a0001c0002t0001g0082others(38): Show | 61 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
splice_region_variant&intron_variant | LOW | c.691-9dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | |||||
chr14:77468051
|
C | CTT | 8 | a0001c0002t0002g0106a0001c0002t0002g0114a0001c0002t0002g0120others(5): Show | 8 | HG01099.hp2 HG01109.hp2 HG01891.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.691-10_691-9dupTT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | |||||
chr14:77468051
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 130 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-32C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77468051 | ||||||
chr14:77468051
|
CT | C | 11 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0033others(8): Show | 14 | HG01169.hp2 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-9delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | |||||
chr14:77468051
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.691-19_691-9delTTT others(8): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 77468051 | |||||
chr14:77468074
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.691-9T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 6/8 | chr14 | 77468074 | ||||||
chr14:77468244
|
T | C | 14 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(11): Show | 35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.792+60T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | chr14 | 77468244 | ||||||
chr14:77468258
|
CTA | C | 11 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0031others(8): Show | 20 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.792+77_792+78delTA | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 77468258 | |||||
chr14:77468374
|
G | A | 4 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(1): Show | 10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-83G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | chr14 | 77468374 | ||||||
chr14:77468415
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.793-42A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 7/8 | chr14 | 77468415 | ||||||
chr14:77468562
|
A | AT | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 158 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.844+73dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468562 | |||||
chr14:77468562
|
A | ATT | 6 | a0001c0001t0001g0014a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 8 | HG01175.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+72_844+73dupTT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468562 | |||||
chr14:77468562
|
AT | A | 15 | a0001c0002t0001g0022a0001c0002t0001g0025a0001c0002t0001g0033others(12): Show | 17 | HG01516.hp1 HG02148.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.844+73delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468562 | |||||
chr14:77468629
|
C | T | 4 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(1): Show | 10 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+121C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468629 | ||||||
chr14:77468685
|
C | T | 2 | a0001c0005t0001g0086a0001c0005t0001g0097 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.844+177C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468685 | ||||||
chr14:77468721
|
C | CT | 6 | a0001c0002t0001g0101a0001c0002t0002g0112a0001c0002t0002g0114others(3): Show | 6 | HG01099.hp2 HG01517.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+237dupT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTT | 12 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0018others(9): Show | 33 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.844+234_844+237dup others(4): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT | 9 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(6): Show | 9 | HG01109.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+231_844+237dup others(7): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(1): Show |
10 | a0001c0002t0001g0008a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 20 | HG00099.hp2 HG01255.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.844+230_844+237dup others(8): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(2): Show |
4 | a0001c0002t0001g0012a0001c0002t0001g0143a0001c0004t0001g0020others(1): Show | 9 | HG00741.hp1 HG01123.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+229_844+237dup others(9): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(3): Show |
2 | a0001c0002t0001g0142a0001c0004t0001g0149 | 2 | HG01243.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.844+228_844+237dup others(10): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844+224_844+237dup others(14): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0001g0085 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.844+223_844+237dup others(15): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(9): Show |
1 | a0001c0002t0001g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.844+222_844+237dup others(16): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(15): Show |
1 | a0001c0005t0001g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.844+216_844+237dup others(22): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
C | CTTTTTTT others(16): Show |
1 | a0001c0005t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.844+215_844+237dup others(23): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
CT | C | 20 | a0001c0001t0001g0058a0001c0002t0001g0132a0001c0002t0001g0133others(17): Show | 32 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.844+237delT | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
CTT | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0074others(5): Show | 13 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+236_844+237del others(2): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
CTTT | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(34): Show | 117 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.844+235_844+237del others(3): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468721
|
CTTTT | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0002t0001g0022others(5): Show | 9 | HG01070.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+234_844+237del others(4): Show |
AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468721 | |||||
chr14:77468743
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.844+235T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468743 | ||||||
chr14:77468744
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.844+236T>C | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468744 | ||||||
chr14:77468745
|
T | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG01106.hp1 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844+237T>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468745 | ||||||
chr14:77468754
|
A | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.844+246A>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468754 | ||||||
chr14:77468755
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.844+247C>T | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468755 | ||||||
chr14:77468802
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 132 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.845-275G>A | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468802 | ||||||
chr14:77468893
|
A | G | 5 | a0001c0004t0001g0010a0001c0004t0001g0020a0001c0004t0001g0149others(2): Show | 11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.845-184A>G | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | chr14 | 77468893 | ||||||
chr14:77468896
|
T | TG | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.845-179dupG | AHSA1 | ENSG00000100591.8 | transcript | ENST00000216479.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 77468896 |