geneid | 79152 |
---|---|
ensemblid | ENSG00000103089.9 |
hgncid | 21197 |
symbol | FA2H |
name | fatty acid 2-hydroxylase |
refseq_nuc | NM_024306.5 |
refseq_prot | NP_077282.3 |
ensembl_nuc | ENST00000219368.8 |
ensembl_prot | ENSP00000219368.3 |
mane_status | MANE Select |
chr | chr16 |
start | 74712969 |
end | 74774820 |
strand | - |
ver | v1.2 |
region | chr16:74712969-74774820 |
region5000 | chr16:74707969-74779820 |
regionname0 | FA2H_chr16_74712969_74774820 |
regionname5000 | FA2H_chr16_74707969_74779820 |
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 | 372 | 379 | 87 | 65 | 164 | 15 | 46 | 124 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002 | 0/0 | 372 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0003 | 0/0 | 372 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0004 | 0/0 | 372 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0005 | 0/0 | 372 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
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 | 1119 | 203 | 27 | 39 | 99 | 8 | 29 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0002 | 1/0 | 1119 | 75 | 6 | 12 | 46 | 2 | 8 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0003 | 0/0 | 1119 | 44 | 26 | 5 | 4 | 4 | 5 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0004 | 0/0 | 1119 | 16 | 10 | 3 | 2 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0005 | 0/0 | 1119 | 14 | 9 | 0 | 5 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0006 | 0/0 | 1119 | 9 | 2 | 5 | 0 | 1 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0007 | 0/0 | 1119 | 6 | 0 | 0 | 6 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0008 | 0/0 | 1119 | 5 | 3 | 1 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0009 | 0/0 | 1119 | 3 | 3 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0010 | 0/0 | 1119 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0011 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0012 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0013 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0014 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0015 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0016 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0017 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0018 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0019 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0020 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
c0021 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
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 | 1287 | 211 | 27 | 26 | 128 | 5 | 23 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0002 | 0/0 | 1287 | 65 | 12 | 26 | 15 | 3 | 9 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0003 | 0/0 | 1287 | 46 | 18 | 7 | 4 | 5 | 12 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0004 | 0/0 | 1287 | 9 | 7 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0005 | 0/0 | 1287 | 7 | 7 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0006 | 0/0 | 1287 | 7 | 1 | 0 | 6 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0007 | 0/0 | 1287 | 5 | 0 | 1 | 3 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0008 | 0/0 | 1287 | 5 | 0 | 0 | 5 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0009 | 0/0 | 1287 | 4 | 4 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0010 | 0/0 | 1287 | 4 | 4 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0011 | 0/0 | 1287 | 3 | 2 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0012 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0013 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0014 | 0/0 | 1287 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0015 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0016 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0017 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0018 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0019 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0020 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0021 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0022 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0023 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0024 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0025 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0026 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0027 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0028 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0029 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
t0030 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
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 | 4 | 0 | 1 | 0 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
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 | 1119 | 203 | 27 | 39 | 99 | 8 | 29 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002 | 1/0 | 1119 | 75 | 6 | 12 | 46 | 2 | 8 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003 | 0/0 | 1119 | 44 | 26 | 5 | 4 | 4 | 5 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004 | 0/0 | 1119 | 16 | 10 | 3 | 2 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005 | 0/0 | 1119 | 14 | 9 | 0 | 5 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0006 | 0/0 | 1119 | 9 | 2 | 5 | 0 | 1 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0007 | 0/0 | 1119 | 6 | 0 | 0 | 6 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0008 | 0/0 | 1119 | 5 | 3 | 1 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0010 | 0/0 | 1119 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0012 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0013 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0014 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0018 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0019 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0009 | 0/0 | 1119 | 3 | 3 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0016 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0017 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0020 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0003c0021 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0004c0015 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0005c0011 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2405 | 115 | 14 | 12 | 73 | 2 | 13 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0002 | 0/0 | 2405 | 42 | 3 | 19 | 15 | 0 | 5 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0003 | 0/0 | 2405 | 29 | 6 | 6 | 4 | 3 | 10 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0005 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0006 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0007 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0008 | 0/0 | 2405 | 3 | 0 | 0 | 3 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0011 | 0/0 | 2405 | 2 | 1 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0014 | 0/0 | 2405 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0018 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0022 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0023 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0024 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0026 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0028 | 0/0 | 2390 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0001t0030 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0001 | 1/0 | 2405 | 63 | 1 | 12 | 42 | 1 | 6 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0002 | 0/0 | 2405 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0003 | 0/0 | 2405 | 5 | 4 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0006 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0008 | 0/0 | 2405 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0015 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0002t0029 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003t0001 | 0/0 | 2405 | 13 | 5 | 1 | 4 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003t0002 | 0/0 | 2405 | 13 | 7 | 3 | 0 | 2 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003t0003 | 0/0 | 2405 | 9 | 5 | 1 | 0 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003t0005 | 0/0 | 2405 | 6 | 6 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003t0009 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0003t0011 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004t0001 | 0/0 | 2405 | 2 | 1 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004t0004 | 0/0 | 2405 | 8 | 6 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004t0006 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004t0007 | 0/0 | 2405 | 3 | 0 | 1 | 1 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004t0019 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0004t0025 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0004 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0006 | 0/0 | 2405 | 4 | 0 | 0 | 4 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0007 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0010 | 0/0 | 2405 | 4 | 4 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0012 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0005t0013 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0006t0001 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0006t0002 | 0/0 | 2405 | 8 | 2 | 4 | 0 | 1 | 1 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0007t0001 | 0/0 | 2405 | 6 | 0 | 0 | 6 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0008t0001 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0008t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0008t0009 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0008t0027 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0010t0001 | 0/0 | 2405 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0012t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0013t0001 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0014t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0018t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0001c0019t0016 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0009t0001 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0009t0012 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0016t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0017t0021 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0002c0020t0017 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0003c0021t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0004c0015t0001 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
a0005c0011t0020 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | copy fasta | chr16 | 74707969 | 74779820 |
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 | 4 | 0 | 1 | 0 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0014g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0018g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0022g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0023g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0024g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0026g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0028g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0030g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0029g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0009g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0011g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0007g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0019g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0025g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0012g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0013g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0009g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0009g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0027g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0010t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0010t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0012t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0013t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0014t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0018t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0019t0016g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0009t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0009t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0009t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0016t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0017t0021g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0020t0017g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0003c0021t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0004c0015t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0005c0011t0020g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0318 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0221 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0184 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00280 | hp2 | a0001 | c0001 | t0011 | g0245 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00323 | hp1 | a0001 | c0001 | t0030 | g0157 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00323 | hp2 | a0001 | c0006 | t0002 | g0342 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0289 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00621 | hp2 | a0001 | c0001 | t0026 | g0039 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00639 | hp1 | a0001 | c0006 | t0002 | g0337 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00735 | hp2 | a0001 | c0006 | t0002 | g0349 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01069 | hp1 | a0001 | c0004 | t0004 | g0298 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01069 | hp2 | a0001 | c0004 | t0007 | g0082 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01071 | hp1 | a0005 | c0011 | t0020 | g0013 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01071 | hp2 | a0001 | c0004 | t0004 | g0297 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01074 | hp2 | a0001 | c0006 | t0002 | g0345 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01192 | hp1 | a0001 | c0006 | t0001 | g0307 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01256 | hp2 | a0001 | c0008 | t0027 | g0348 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01257 | hp1 | a0001 | c0003 | t0002 | g0314 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0340 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0313 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01358 | hp1 | a0001 | c0003 | t0003 | g0011 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0217 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0206 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01516 | hp1 | a0004 | c0015 | t0001 | g0302 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0010 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01517 | hp1 | a0001 | c0003 | t0002 | g0010 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0220 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01884 | hp2 | a0001 | c0019 | t0016 | g0366 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0356 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01975 | hp1 | a0001 | c0001 | t0014 | g0079 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0308 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02040 | hp2 | a0001 | c0005 | t0007 | g0332 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02055 | hp2 | a0001 | c0004 | t0004 | g0279 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02071 | hp1 | a0001 | c0007 | t0001 | g0038 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0057 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02145 | hp1 | a0001 | c0008 | t0009 | g0372 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02145 | hp2 | a0001 | c0008 | t0003 | g0358 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02257 | hp1 | a0001 | c0005 | t0012 | g0368 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02257 | hp2 | a0001 | c0003 | t0003 | g0341 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02258 | hp1 | a0001 | c0002 | t0015 | g0198 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0321 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02293 | hp2 | a0001 | c0001 | t0014 | g0033 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02451 | hp1 | a0001 | c0003 | t0003 | g0324 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02451 | hp2 | a0001 | c0018 | t0003 | g0336 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02572 | hp1 | a0001 | c0008 | t0009 | g0373 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02572 | hp2 | a0001 | c0003 | t0009 | g0353 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02615 | hp2 | a0001 | c0003 | t0005 | g0305 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0329 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02647 | hp2 | a0001 | c0003 | t0005 | g0369 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0339 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0333 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02717 | hp1 | a0001 | c0003 | t0005 | g0361 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02717 | hp2 | a0001 | c0004 | t0004 | g0280 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02738 | hp2 | a0001 | c0003 | t0003 | g0351 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02809 | hp1 | a0001 | c0005 | t0010 | g0325 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0334 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02818 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02886 | hp1 | a0001 | c0012 | t0001 | g0014 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02886 | hp2 | a0001 | c0001 | t0024 | g0022 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0322 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02895 | hp2 | a0001 | c0006 | t0002 | g0344 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0320 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02896 | hp2 | a0002 | c0009 | t0001 | g0215 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02897 | hp1 | a0001 | c0006 | t0002 | g0343 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02897 | hp2 | a0002 | c0009 | t0001 | g0213 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0352 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02922 | hp2 | a0001 | c0003 | t0005 | g0367 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0127 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0371 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02970 | hp2 | a0002 | c0016 | t0001 | g0214 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02976 | hp1 | a0001 | c0003 | t0002 | g0357 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0124 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03041 | hp2 | a0002 | c0020 | t0017 | g0360 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0365 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0328 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03130 | hp2 | a0001 | c0001 | t0023 | g0296 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03225 | hp1 | a0001 | c0004 | t0004 | g0301 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0304 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03453 | hp1 | a0003 | c0021 | t0001 | g0374 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03453 | hp2 | a0001 | c0004 | t0004 | g0210 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03486 | hp2 | a0001 | c0003 | t0003 | g0362 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03490 | hp1 | a0001 | c0010 | t0001 | g0228 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03492 | hp2 | a0001 | c0010 | t0001 | g0248 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03516 | hp1 | a0001 | c0005 | t0010 | g0330 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0123 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03579 | hp1 | a0001 | c0005 | t0013 | g0012 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03579 | hp2 | a0001 | c0003 | t0005 | g0370 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03654 | hp1 | a0001 | c0006 | t0002 | g0347 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03669 | hp2 | a0001 | c0004 | t0007 | g0100 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0335 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03710 | hp1 | a0001 | c0001 | t0018 | g0272 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0255 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04199 | hp2 | a0001 | c0003 | t0003 | g0350 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0292 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18522 | hp2 | a0001 | c0005 | t0013 | g0012 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18612 | hp1 | a0001 | c0002 | t0008 | g0171 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0364 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0327 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18939 | hp2 | a0001 | c0002 | t0008 | g0103 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18946 | hp1 | a0001 | c0007 | t0001 | g0142 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18946 | hp2 | a0001 | c0001 | t0028 | g0046 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18947 | hp1 | a0001 | c0007 | t0001 | g0141 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18948 | hp1 | a0001 | c0005 | t0006 | g0312 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18959 | hp1 | a0001 | c0005 | t0006 | g0306 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0316 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0317 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0319 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18999 | hp2 | a0001 | c0008 | t0001 | g0311 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19000 | hp1 | a0001 | c0005 | t0006 | g0309 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19003 | hp2 | a0001 | c0001 | t0008 | g0136 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19004 | hp2 | a0001 | c0007 | t0001 | g0036 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19007 | hp2 | a0001 | c0005 | t0006 | g0310 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19011 | hp2 | a0001 | c0013 | t0001 | g0106 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19030 | hp2 | a0001 | c0003 | t0011 | g0363 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0338 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19043 | hp2 | a0001 | c0004 | t0025 | g0211 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19054 | hp1 | a0001 | c0004 | t0007 | g0050 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19056 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19064 | hp2 | a0001 | c0002 | t0029 | g0200 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0315 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19074 | hp2 | a0001 | c0002 | t0006 | g0273 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19077 | hp1 | a0001 | c0007 | t0001 | g0143 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19079 | hp2 | a0001 | c0007 | t0001 | g0035 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19080 | hp2 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19085 | hp2 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19240 | hp1 | a0001 | c0005 | t0010 | g0326 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | ASW | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | ASW | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20752 | hp1 | a0001 | c0001 | t0022 | g0240 | EUR | TSI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20752 | hp2 | a0001 | c0003 | t0003 | g0011 | EUR | TSI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | GIH | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | GIH | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01123 | hp2 | a0001 | c0006 | t0002 | g0346 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02109 | hp1 | a0001 | c0005 | t0010 | g0331 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02109 | hp2 | a0001 | c0014 | t0003 | g0129 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02486 | hp1 | a0001 | c0004 | t0019 | g0281 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02486 | hp2 | a0001 | c0005 | t0004 | g0323 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02559 | hp2 | a0002 | c0017 | t0021 | g0021 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03471 | hp1 | a0002 | c0009 | t0012 | g0088 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03471 | hp2 | a0001 | c0003 | t0009 | g0354 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0359 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0300 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0355 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA21309 | hp2 | a0001 | c0004 | t0006 | g0025 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0051 | REF | REF | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0125 | REF | REF | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74718989
|
T | G | 1 | a0004 | 1 | HG01516.hp1 | missense_variant&splice_region_variant | MODERATE | c.785A>C | p.Lys262Thr | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/7 | 850/2405 | 785/1119 | 262/372 | chr16 | 74718989 | ||
chr16:74740097
|
G | C | 1 | a0002 | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.289C>G | p.Pro97Ala | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/7 | 354/2405 | 289/1119 | 97/372 | chr16 | 74740097 | ||
chr16:74774625
|
G | T | 1 | a0005 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.131C>A | p.Pro44Gln | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 196/2405 | 131/1119 | 44/372 | chr16 | 74774625 | ||
chr16:74774671
|
G | C | 1 | a0003 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.85C>G | p.Arg29Gly | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 150/2405 | 85/1119 | 29/372 | chr16 | 74774671 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74714196
|
C | G | 2 | a0001c0014a0001c0018 | 2 | HG02109.hp2 HG02451.hp2 |
synonymous_variant | LOW | c.1113G>C | p.Thr371Thr | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1178/2405 | 1113/1119 | 371/372 | chr16 | 74714196 | ||
chr16:74716417
|
C | T | 1 | a0001c0013 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.969G>A | p.Pro323Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 1034/2405 | 969/1119 | 323/372 | chr16 | 74716417 | ||
chr16:74716453
|
A | G | 3 | a0001c0004a0001c0005a0002c0009 | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
synonymous_variant | LOW | c.933T>C | p.Tyr311Tyr | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 998/2405 | 933/1119 | 311/372 | chr16 | 74716453 | ||
chr16:74716498
|
T | C | 5 | a0001c0004a0001c0005a0001c0006others(2): Show | 44 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
synonymous_variant | LOW | c.888A>G | p.Val296Val | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 953/2405 | 888/1119 | 296/372 | chr16 | 74716498 | ||
chr16:74716507
|
G | A | 12 | a0001c0001a0001c0003a0001c0006others(9): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
synonymous_variant | LOW | c.879C>T | p.Pro293Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 944/2405 | 879/1119 | 293/372 | chr16 | 74716507 | ||
chr16:74726301
|
C | T | 1 | a0001c0007 | 6 | HG02071.hp1 NA18946.hp1 NA18947.hp1 others(3): Show |
synonymous_variant | LOW | c.537G>A | p.Leu179Leu | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/7 | 602/2405 | 537/1119 | 179/372 | chr16 | 74726301 | ||
chr16:74727306
|
C | A | 1 | a0001c0019 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.444G>T | p.Pro148Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/7 | 509/2405 | 444/1119 | 148/372 | chr16 | 74727306 | ||
chr16:74774527
|
G | A | 8 | a0001c0003a0001c0005a0001c0006others(5): Show | 76 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(73): Show |
synonymous_variant | LOW | c.229C>T | p.Leu77Leu | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 294/2405 | 229/1119 | 77/372 | chr16 | 74774527 | ||
chr16:74774558
|
C | G | 1 | a0001c0012 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.198G>C | p.Pro66Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 263/2405 | 198/1119 | 66/372 | chr16 | 74774558 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74713059
|
T | G | 10 | a0001c0001t0005a0001c0001t0023a0001c0001t0024others(7): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1131A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1131 | chr16 | 74713059 | |||||
chr16:74713061
|
C | T | 2 | a0001c0001t0024a0001c0005t0010 | 5 | HG02109.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1129G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1129 | chr16 | 74713061 | |||||
chr16:74713123
|
C | T | 1 | a0001c0004t0019 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1067 | chr16 | 74713123 | |||||
chr16:74713126
|
G | C | 22 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(19): Show | 75 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1064C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1064 | chr16 | 74713126 | |||||
chr16:74713232
|
G | A | 1 | a0001c0005t0013 | 2 | HG03579.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*958C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 958 | chr16 | 74713232 | |||||
chr16:74713353
|
G | A | 1 | a0001c0001t0026 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*837C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 837 | chr16 | 74713353 | |||||
chr16:74713369
|
G | C | 1 | a0001c0008t0027 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 821 | chr16 | 74713369 | |||||
chr16:74713369
|
GGGGAGGT others(8): Show |
G | 1 | a0001c0001t0028 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806_*820delAGTGCC others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 806 | chr16 | 74713369 | |||||
chr16:74713377
|
G | A | 1 | a0001c0001t0014 | 2 | HG01975.hp1 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*813C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 813 | chr16 | 74713377 | |||||
chr16:74713407
|
C | T | 2 | a0001c0001t0008a0001c0002t0008 | 5 | NA18612.hp1 NA18939.hp2 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*783G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 783 | chr16 | 74713407 | |||||
chr16:74713553
|
C | G | 12 | a0001c0001t0002a0001c0001t0011a0001c0001t0014others(9): Show | 75 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*637G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 637 | chr16 | 74713553 | |||||
chr16:74713594
|
T | G | 1 | a0001c0002t0029 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*596A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 596 | chr16 | 74713594 | |||||
chr16:74713650
|
G | A | 1 | a0001c0001t0030 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 540 | chr16 | 74713650 | |||||
chr16:74713670
|
C | T | 1 | a0001c0001t0022 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*520G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 520 | chr16 | 74713670 | |||||
chr16:74713786
|
A | T | 16 | a0001c0001t0006a0001c0001t0007a0001c0002t0006others(13): Show | 32 | HG00438.hp2 HG01069.hp1 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*404T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 404 | chr16 | 74713786 | |||||
chr16:74713907
|
C | G | 12 | a0001c0001t0005a0001c0001t0018a0001c0003t0005others(9): Show | 27 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*283G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 283 | chr16 | 74713907 | |||||
chr16:74713909
|
G | T | 12 | a0001c0001t0005a0001c0001t0018a0001c0003t0005others(9): Show | 27 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*281C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 281 | chr16 | 74713909 | |||||
chr16:74713947
|
C | T | 4 | a0001c0001t0005a0001c0001t0018a0001c0003t0005others(1): Show | 9 | HG02615.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*243G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 243 | chr16 | 74713947 | |||||
chr16:74714156
|
C | T | 2 | a0001c0002t0015a0001c0019t0016 | 2 | HG01884.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*34G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 34 | chr16 | 74714156 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74714447
|
T | C | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1040-178A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714447 | ||||||
chr16:74714531
|
C | T | 1 | a0001c0001t0011g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1040-262G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714531 | ||||||
chr16:74714725
|
A | G | 17 | a0001c0004t0001g0057a0001c0004t0007g0050a0001c0004t0007g0082others(14): Show | 17 | HG01069.hp2 HG01884.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1040-456T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714725 | ||||||
chr16:74714825
|
G | C | 3 | a0001c0005t0012g0368a0001c0005t0013g0012a0002c0009t0012g0088 | 4 | HG02257.hp1 HG03471.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-556C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714825 | ||||||
chr16:74714834
|
AT | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0260a0001c0001t0001g0286others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.1040-566delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714834 | ||||||
chr16:74714834
|
ATT | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 94 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1040-567_1040-566d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714834 | ||||||
chr16:74714834
|
ATTT | A | 20 | a0001c0001t0001g0072a0001c0001t0001g0151a0001c0004t0001g0057others(17): Show | 20 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1040-568_1040-566d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714834 | ||||||
chr16:74714871
|
T | C | 4 | a0001c0005t0006g0306a0001c0005t0006g0309a0001c0005t0006g0310others(1): Show | 4 | NA18948.hp1 NA18959.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-602A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714871 | ||||||
chr16:74714983
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1040-714G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714983 | ||||||
chr16:74715024
|
GA | G | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040-756delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715024 | ||||||
chr16:74715239
|
T | A | 1 | a0001c0003t0003g0351 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1040-970A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715239 | ||||||
chr16:74715362
|
GC | G | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+984delG | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715362 | ||||||
chr16:74715492
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1039+855A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715492 | ||||||
chr16:74715545
|
G | A | 15 | a0001c0004t0001g0300a0001c0004t0004g0009a0001c0004t0004g0210others(12): Show | 17 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039+802C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715545 | ||||||
chr16:74715687
|
G | A | 1 | a0001c0005t0010g0326 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1039+660C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715687 | ||||||
chr16:74715768
|
C | G | 6 | a0001c0001t0002g0236a0001c0001t0002g0241a0001c0001t0002g0261others(3): Show | 6 | HG00735.hp1 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+579G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715768 | ||||||
chr16:74715790
|
C | T | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+557G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715790 | ||||||
chr16:74715794
|
C | T | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+553G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715794 | ||||||
chr16:74715799
|
C | T | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+548G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715799 | ||||||
chr16:74715800
|
T | TTTC | 11 | a0001c0004t0001g0057a0001c0004t0007g0100a0001c0005t0006g0306others(8): Show | 11 | HG02040.hp2 HG02109.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039+544_1039+546d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715800 | ||||||
chr16:74715812
|
C | CTTTTTTT others(16): Show |
3 | a0001c0004t0001g0300a0002c0009t0001g0213a0002c0009t0001g0215 | 3 | HG02896.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1039+534_1039+535i others(25): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715812 | ||||||
chr16:74715815
|
C | T | 14 | a0001c0004t0001g0300a0001c0004t0004g0009a0001c0004t0004g0210others(11): Show | 16 | HG01071.hp2 HG02055.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1039+532G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715815 | ||||||
chr16:74715815
|
CT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0070a0001c0001t0001g0282others(8): Show | 11 | HG00738.hp1 HG01981.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039+531delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715815 | ||||||
chr16:74715818
|
T | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0146 | 2 | NA19011.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1039+529A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715818 | ||||||
chr16:74715832
|
T | A | 36 | a0001c0001t0005g0188a0001c0003t0003g0329a0001c0003t0005g0305others(33): Show | 38 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1039+515A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715832 | ||||||
chr16:74715854
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 118 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1039+493A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715854 | ||||||
chr16:74715855
|
G | A | 45 | a0001c0001t0005g0188a0001c0003t0003g0329a0001c0003t0005g0305others(42): Show | 47 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1039+492C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715855 | ||||||
chr16:74715876
|
T | C | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+471A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715876 | ||||||
chr16:74715958
|
G | A | 1 | a0001c0002t0029g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1039+389C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715958 | ||||||
chr16:74716004
|
C | T | 27 | a0001c0004t0001g0057a0001c0004t0004g0009a0001c0004t0004g0210others(24): Show | 29 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1039+343G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716004 | ||||||
chr16:74716105
|
C | T | 13 | a0001c0004t0001g0057a0001c0004t0007g0050a0001c0004t0007g0082others(10): Show | 13 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039+242G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716105 | ||||||
chr16:74716209
|
G | A | 1 | a0001c0004t0007g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1039+138C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716209 | ||||||
chr16:74716219
|
T | C | 2 | a0001c0002t0001g0107a0001c0002t0001g0212 | 2 | HG02080.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1039+128A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716219 | ||||||
chr16:74716236
|
A | G | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+111T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716236 | ||||||
chr16:74716244
|
C | A | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+103G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716244 | ||||||
chr16:74716245
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1039+102C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716245 | ||||||
chr16:74716285
|
G | A | 1 | a0001c0006t0002g0347 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1039+62C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716285 | ||||||
chr16:74716331
|
A | C | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+16T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716331 | ||||||
chr16:74716339
|
A | G | 41 | a0001c0002t0003g0123a0001c0002t0003g0124a0001c0002t0003g0127others(38): Show | 43 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.1039+8T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716339 | ||||||
chr16:74716658
|
A | G | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-59T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716658 | ||||||
chr16:74716695
|
G | A | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-96C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716695 | ||||||
chr16:74716748
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.787-149C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716748 | ||||||
chr16:74716757
|
C | T | 5 | a0001c0004t0025g0211a0001c0005t0001g0365a0001c0005t0012g0368others(2): Show | 6 | HG02257.hp1 HG03098.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-158G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716757 | ||||||
chr16:74716788
|
T | C | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-189A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716788 | ||||||
chr16:74716832
|
C | T | 2 | a0001c0005t0001g0365a0001c0005t0013g0012 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.787-233G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716832 | ||||||
chr16:74716976
|
A | G | 13 | a0001c0004t0001g0057a0001c0004t0007g0050a0001c0004t0007g0082others(10): Show | 13 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.787-377T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716976 | ||||||
chr16:74717048
|
A | G | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-449T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717048 | ||||||
chr16:74717049
|
A | G | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-450T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717049 | ||||||
chr16:74717074
|
C | G | 13 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(10): Show | 15 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.787-475G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717074 | ||||||
chr16:74717084
|
C | T | 4 | a0001c0001t0001g0061a0001c0004t0001g0300a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-485G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717084 | ||||||
chr16:74717269
|
G | A | 1 | a0001c0007t0001g0035 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.787-670C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717269 | ||||||
chr16:74717328
|
A | G | 31 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(28): Show | 33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-729T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717328 | ||||||
chr16:74717334
|
T | G | 12 | a0001c0001t0003g0126a0001c0006t0001g0307a0001c0006t0002g0337others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.787-735A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717334 | ||||||
chr16:74717375
|
G | C | 4 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0003g0255others(1): Show | 4 | HG03710.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-776C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717375 | ||||||
chr16:74717383
|
A | G | 43 | a0001c0001t0003g0126a0001c0004t0001g0057a0001c0004t0001g0300others(40): Show | 45 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.787-784T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717383 | ||||||
chr16:74717496
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.787-897G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717496 | ||||||
chr16:74717505
|
G | A | 30 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(27): Show | 31 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.787-906C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717505 | ||||||
chr16:74717530
|
G | A | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.787-931C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717530 | ||||||
chr16:74717532
|
T | C | 42 | a0001c0004t0001g0057a0001c0004t0001g0300a0001c0004t0004g0009others(39): Show | 44 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.787-933A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717532 | ||||||
chr16:74717634
|
A | T | 27 | a0001c0004t0001g0057a0001c0004t0004g0009a0001c0004t0004g0210others(24): Show | 29 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.787-1035T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717634 | ||||||
chr16:74717680
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.787-1081G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717680 | ||||||
chr16:74717722
|
G | C | 1 | a0001c0002t0001g0122 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.787-1123C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717722 | ||||||
chr16:74717830
|
G | A | 14 | a0001c0001t0005g0188a0001c0003t0003g0329a0001c0003t0005g0305others(11): Show | 14 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+1158C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717830 | ||||||
chr16:74717929
|
G | C | 13 | a0001c0004t0001g0057a0001c0004t0007g0050a0001c0004t0007g0082others(10): Show | 13 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+1059C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717929 | ||||||
chr16:74718027
|
C | G | 1 | a0001c0002t0001g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.786+961G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718027 | ||||||
chr16:74718028
|
C | G | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.786+960G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718028 | ||||||
chr16:74718203
|
C | T | 1 | a0001c0005t0010g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.786+785G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718203 | ||||||
chr16:74718244
|
A | G | 10 | a0001c0002t0003g0123a0001c0002t0003g0124a0001c0002t0003g0127others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.786+744T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718244 | ||||||
chr16:74718261
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.786+727T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718261 | ||||||
chr16:74718273
|
A | G | 15 | a0001c0001t0003g0126a0001c0001t0005g0188a0001c0003t0003g0329others(12): Show | 15 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+715T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718273 | ||||||
chr16:74718278
|
T | C | 25 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(22): Show | 27 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+710A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718278 | ||||||
chr16:74718298
|
G | T | 1 | a0001c0003t0003g0324 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.786+690C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718298 | ||||||
chr16:74718312
|
G | C | 12 | a0001c0001t0003g0126a0001c0006t0001g0307a0001c0006t0002g0337others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.786+676C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718312 | ||||||
chr16:74718327
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.786+661A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718327 | ||||||
chr16:74718418
|
G | A | 1 | a0001c0003t0005g0367 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.786+570C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718418 | ||||||
chr16:74718594
|
T | G | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+394A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718594 | ||||||
chr16:74718624
|
C | G | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+364G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718624 | ||||||
chr16:74718625
|
G | A | 1 | a0001c0001t0018g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.786+363C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718625 | ||||||
chr16:74718637
|
G | C | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.786+351C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718637 | ||||||
chr16:74718672
|
G | A | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.786+316C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718672 | ||||||
chr16:74718706
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.786+282A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718706 | ||||||
chr16:74718707
|
G | C | 1 | a0002c0017t0021g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.786+281C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718707 | ||||||
chr16:74718750
|
C | T | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.786+238G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718750 | ||||||
chr16:74718846
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.786+142G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718846 | ||||||
chr16:74718923
|
G | C | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+65C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718923 | ||||||
chr16:74718943
|
C | G | 39 | a0001c0001t0001g0083a0001c0002t0015g0198a0001c0004t0004g0009others(36): Show | 41 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.786+45G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718943 | ||||||
chr16:74719167
|
G | C | 1 | a0001c0001t0003g0126 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.614-7C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719167 | ||||||
chr16:74719181
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.614-21G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719181 | ||||||
chr16:74719217
|
C | T | 2 | a0001c0002t0015g0198a0001c0019t0016g0366 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.614-57G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719217 | ||||||
chr16:74719224
|
C | T | 4 | a0001c0004t0001g0300a0001c0004t0006g0025a0002c0009t0001g0213others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-64G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719224 | ||||||
chr16:74719249
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.614-89G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719249 | ||||||
chr16:74719570
|
G | A | 5 | a0001c0002t0001g0182a0001c0002t0001g0185a0001c0002t0001g0186others(2): Show | 5 | HG01361.hp1 HG01496.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-410C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719570 | ||||||
chr16:74719592
|
C | T | 14 | a0001c0001t0005g0188a0001c0003t0003g0329a0001c0003t0005g0305others(11): Show | 14 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.614-432G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719592 | ||||||
chr16:74719802
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.614-642G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719802 | ||||||
chr16:74720082
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.614-922G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720082 | ||||||
chr16:74720125
|
A | G | 13 | a0001c0004t0001g0300a0001c0004t0004g0009a0001c0004t0004g0210others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.614-965T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720125 | ||||||
chr16:74720139
|
T | A | 1 | a0002c0017t0021g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.614-979A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720139 | ||||||
chr16:74720145
|
C | G | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-985G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720145 | ||||||
chr16:74720162
|
CAT | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.614-1004_614-1003d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720162 | ||||||
chr16:74720165
|
A | AT | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.614-1006dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720165 | ||||||
chr16:74720167
|
A | C | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.614-1007T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720167 | ||||||
chr16:74720180
|
C | CT | 36 | a0001c0002t0001g0048a0001c0002t0001g0089a0001c0002t0001g0095others(33): Show | 36 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.614-1021dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
C | CTT | 12 | a0001c0002t0001g0094a0001c0002t0001g0165a0001c0003t0001g0318others(9): Show | 14 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.614-1022_614-1021d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
C | CTTT | 6 | a0001c0002t0001g0015a0001c0003t0003g0329a0001c0003t0005g0361others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1023_614-1021d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
C | CTTTT | 7 | a0001c0001t0005g0188a0001c0002t0003g0127a0001c0002t0003g0304others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1024_614-1021d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
C | CTTTTT | 6 | a0001c0001t0003g0126a0001c0002t0003g0123a0001c0002t0003g0124others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1025_614-1021d others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
C | CTTTTTTT others(3): Show |
1 | a0001c0006t0002g0349 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.614-1030_614-1021d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
CT | C | 75 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0040others(72): Show | 77 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.614-1021delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
CTT | C | 88 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0032others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.614-1022_614-1021d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
CTTT | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0076others(10): Show | 13 | HG00408.hp2 HG00621.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-1023_614-1021d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
CTTTT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(49): Show | 57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.614-1024_614-1021d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720180
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.614-1030_614-1021d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | ||||||
chr16:74720357
|
G | C | 2 | a0001c0001t0001g0237a0001c0001t0003g0232 | 2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.614-1197C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720357 | ||||||
chr16:74720384
|
G | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.614-1224C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720384 | ||||||
chr16:74720442
|
C | T | 1 | a0001c0003t0003g0324 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-1282G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720442 | ||||||
chr16:74720583
|
C | T | 2 | a0001c0003t0002g0352a0001c0012t0001g0014 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.614-1423G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720583 | ||||||
chr16:74720623
|
A | T | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-1463T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720623 | ||||||
chr16:74720664
|
C | T | 2 | a0001c0003t0001g0321a0001c0003t0001g0359 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.614-1504G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720664 | ||||||
chr16:74720678
|
T | G | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-1518A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720678 | ||||||
chr16:74720680
|
A | G | 1 | a0001c0002t0001g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.614-1520T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720680 | ||||||
chr16:74720720
|
T | C | 4 | a0001c0003t0009g0353a0001c0003t0009g0354a0001c0008t0009g0372others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-1560A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720720 | ||||||
chr16:74721198
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.614-2038C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721198 | ||||||
chr16:74721231
|
G | A | 2 | a0001c0005t0001g0365a0001c0005t0013g0012 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.614-2071C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721231 | ||||||
chr16:74721281
|
C | T | 3 | a0001c0003t0002g0355a0001c0003t0002g0356a0001c0003t0002g0357 | 3 | HG01891.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.614-2121G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721281 | ||||||
chr16:74721365
|
A | C | 1 | a0001c0013t0001g0106 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.614-2205T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721365 | ||||||
chr16:74721447
|
A | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.614-2287T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721447 | ||||||
chr16:74721554
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.614-2394C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721554 | ||||||
chr16:74721613
|
T | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0026others(187): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.614-2453A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721613 | ||||||
chr16:74721686
|
T | G | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-2526A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721686 | ||||||
chr16:74721732
|
C | G | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.614-2572G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721732 | ||||||
chr16:74721887
|
G | A | 12 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-2727C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721887 | ||||||
chr16:74721906
|
A | G | 3 | a0001c0001t0003g0008a0001c0001t0003g0244a0001c0001t0011g0245 | 4 | HG00280.hp2 HG01255.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-2746T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721906 | ||||||
chr16:74722032
|
G | A | 25 | a0001c0001t0003g0126a0001c0004t0001g0300a0001c0004t0004g0009others(22): Show | 26 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.614-2872C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722032 | ||||||
chr16:74722065
|
A | T | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-2905T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722065 | ||||||
chr16:74722068
|
C | A | 1 | a0001c0002t0001g0183 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.614-2908G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722068 | ||||||
chr16:74722189
|
T | C | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.614-3029A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722189 | ||||||
chr16:74722220
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.614-3060G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722220 | ||||||
chr16:74722554
|
G | A | 48 | a0001c0002t0003g0123a0001c0002t0003g0124a0001c0002t0003g0127others(45): Show | 51 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.614-3394C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722554 | ||||||
chr16:74722825
|
C | T | 1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.613+3400G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722825 | ||||||
chr16:74722911
|
C | CA | 15 | a0001c0001t0001g0285a0001c0002t0001g0108a0001c0002t0001g0133others(12): Show | 15 | HG01884.hp2 HG01952.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.613+3313dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | ||||||
chr16:74722911
|
CA | C | 14 | a0001c0001t0005g0188a0001c0002t0001g0053a0001c0003t0005g0361others(11): Show | 16 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.613+3313delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | ||||||
chr16:74722911
|
CAA | C | 6 | a0001c0001t0001g0151a0001c0001t0001g0268a0001c0001t0002g0092others(3): Show | 6 | HG01243.hp2 HG01978.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+3312_613+3313d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | ||||||
chr16:74722911
|
CAAA | C | 163 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0030others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.613+3311_613+3313d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | ||||||
chr16:74722911
|
CAAAA | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 76 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.613+3310_613+3313d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | ||||||
chr16:74723027
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.613+3198G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723027 | ||||||
chr16:74723085
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.613+3140C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723085 | ||||||
chr16:74723111
|
G | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0284a0001c0001t0001g0287others(3): Show | 6 | HG00408.hp1 HG00438.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+3114C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723111 | ||||||
chr16:74723227
|
C | T | 2 | a0001c0005t0001g0365a0001c0005t0013g0012 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.613+2998G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723227 | ||||||
chr16:74723349
|
G | A | 2 | a0001c0005t0001g0365a0001c0005t0013g0012 | 3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.613+2876C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723349 | ||||||
chr16:74723369
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.613+2856A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723369 | ||||||
chr16:74723407
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0093a0001c0001t0001g0233others(2): Show | 5 | NA18943.hp2 NA18950.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+2818G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723407 | ||||||
chr16:74723412
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613+2813C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723412 | ||||||
chr16:74723420
|
A | C | 1 | a0001c0001t0002g0041 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.613+2805T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723420 | ||||||
chr16:74723688
|
C | A | 4 | a0001c0002t0015g0198a0001c0005t0001g0365a0001c0005t0013g0012others(1): Show | 5 | HG01884.hp2 HG02258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+2537G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723688 | ||||||
chr16:74723732
|
G | C | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.613+2493C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723732 | ||||||
chr16:74723820
|
G | A | 176 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0030others(173): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.613+2405C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723820 | ||||||
chr16:74724233
|
A | G | 1 | a0001c0003t0005g0367 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.613+1992T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724233 | ||||||
chr16:74724251
|
C | T | 1 | a0001c0001t0008g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.613+1974G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724251 | ||||||
chr16:74724404
|
C | T | 1 | a0001c0002t0003g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.613+1821G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724404 | ||||||
chr16:74724435
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.613+1790A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724435 | ||||||
chr16:74724465
|
G | A | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+1760C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724465 | ||||||
chr16:74724571
|
T | G | 1 | a0001c0003t0001g0315 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.613+1654A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724571 | ||||||
chr16:74724603
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.613+1622G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724603 | ||||||
chr16:74724740
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.613+1485A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724740 | ||||||
chr16:74724755
|
A | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.613+1470T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724755 | ||||||
chr16:74724797
|
C | G | 1 | a0001c0003t0005g0367 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.613+1428G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724797 | ||||||
chr16:74724809
|
A | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.613+1416T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724809 | ||||||
chr16:74724912
|
C | T | 1 | a0002c0009t0012g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.613+1313G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724912 | ||||||
chr16:74724916
|
G | A | 2 | a0001c0005t0012g0368a0002c0009t0012g0088 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.613+1309C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724916 | ||||||
chr16:74725013
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0081 | 2 | NA18942.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.613+1212G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725013 | ||||||
chr16:74725086
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.613+1139T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725086 | ||||||
chr16:74725233
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.613+992C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725233 | ||||||
chr16:74725243
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.613+982G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725243 | ||||||
chr16:74725318
|
C | T | 4 | a0001c0002t0015g0198a0001c0005t0013g0012a0001c0008t0003g0358others(1): Show | 5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+907G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725318 | ||||||
chr16:74725350
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.613+875T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725350 | ||||||
chr16:74725421
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.613+804C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725421 | ||||||
chr16:74725492
|
C | T | 33 | a0001c0003t0002g0010a0001c0004t0004g0009a0001c0004t0004g0210others(30): Show | 35 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.613+733G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725492 | ||||||
chr16:74725531
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(58): Show | 66 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.613+694G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725531 | ||||||
chr16:74725532
|
G | A | 1 | a0001c0003t0001g0319 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.613+693C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725532 | ||||||
chr16:74725608
|
C | T | 5 | a0001c0002t0015g0198a0001c0005t0001g0365a0001c0005t0013g0012others(2): Show | 6 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+617G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725608 | ||||||
chr16:74725656
|
G | A | 1 | a0001c0004t0004g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.613+569C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725656 | ||||||
chr16:74725682
|
C | T | 1 | a0001c0003t0003g0351 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.613+543G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725682 | ||||||
chr16:74725691
|
G | A | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.613+534C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725691 | ||||||
chr16:74725752
|
C | T | 11 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+473G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725752 | ||||||
chr16:74725926
|
G | A | 1 | a0001c0003t0001g0333 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.613+299C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725926 | ||||||
chr16:74726363
|
C | A | 1 | a0001c0001t0001g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507-32G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726363 | ||||||
chr16:74726394
|
CT | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.507-64delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726394 | ||||||
chr16:74726423
|
T | C | 12 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.507-92A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726423 | ||||||
chr16:74726523
|
G | C | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.507-192C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726523 | ||||||
chr16:74726687
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(62): Show | 70 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.507-356C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726687 | ||||||
chr16:74726968
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.506+276C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726968 | ||||||
chr16:74726969
|
C | A | 14 | a0001c0001t0001g0083a0001c0001t0002g0295a0001c0003t0001g0320others(11): Show | 14 | HG01891.hp1 HG02280.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+275G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726969 | ||||||
chr16:74726970
|
G | A | 1 | a0001c0005t0007g0332 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506+274C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726970 | ||||||
chr16:74726998
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.506+246T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726998 | ||||||
chr16:74727424
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.364-38G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727424 | ||||||
chr16:74727587
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364-201C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727587 | ||||||
chr16:74727595
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.364-209A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727595 | ||||||
chr16:74727626
|
G | A | 1 | a0001c0005t0001g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-240C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727626 | ||||||
chr16:74727755
|
G | A | 5 | a0001c0001t0003g0126a0001c0002t0003g0123a0001c0002t0003g0124others(2): Show | 5 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-369C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727755 | ||||||
chr16:74727797
|
TAAAGTCT others(20): Show |
T | 1 | a0001c0002t0001g0104 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.364-438_364-412del others(27): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727797 | ||||||
chr16:74727935
|
T | A | 1 | a0001c0002t0001g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.364-549A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727935 | ||||||
chr16:74727945
|
A | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(41): Show | 46 | HG00621.hp1 HG01975.hp1 HG02040.hp1 others(43): Show |
intron_variant | MODIFIER | c.364-559T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727945 | ||||||
chr16:74728006
|
C | A | 1 | a0001c0001t0002g0277 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.364-620G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728006 | ||||||
chr16:74728087
|
A | G | 1 | a0001c0001t0028g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.364-701T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728087 | ||||||
chr16:74728239
|
T | C | 12 | a0001c0006t0001g0307a0001c0006t0002g0337a0001c0006t0002g0342others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-853A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728239 | ||||||
chr16:74728250
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.364-864A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728250 | ||||||
chr16:74728266
|
T | C | 5 | a0001c0001t0003g0126a0001c0002t0003g0123a0001c0002t0003g0124others(2): Show | 5 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-880A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728266 | ||||||
chr16:74728266
|
T | G | 1 | a0001c0002t0002g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364-880A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728266 | ||||||
chr16:74728570
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.364-1184T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728570 | ||||||
chr16:74728722
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.364-1336G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728722 | ||||||
chr16:74728758
|
T | C | 1 | a0001c0002t0001g0110 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.364-1372A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728758 | ||||||
chr16:74728780
|
C | CT | 11 | a0001c0001t0001g0037a0001c0001t0001g0153a0001c0001t0001g0208others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1395dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728780 | ||||||
chr16:74728780
|
CT | C | 47 | a0001c0001t0001g0042a0001c0001t0001g0066a0001c0001t0001g0071others(44): Show | 48 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.364-1395delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728780 | ||||||
chr16:74728780
|
CTT | C | 33 | a0001c0001t0003g0126a0001c0002t0003g0123a0001c0002t0003g0124others(30): Show | 35 | HG00099.hp2 HG00323.hp2 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.364-1396_364-1395d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728780 | ||||||
chr16:74728784
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.364-1398A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728784 | ||||||
chr16:74728932
|
A | T | 1 | a0001c0002t0001g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.364-1546T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728932 | ||||||
chr16:74729004
|
A | AT | 74 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0074others(71): Show | 78 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.364-1619dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | ||||||
chr16:74729004
|
A | ATT | 16 | a0001c0001t0002g0236a0001c0001t0002g0241a0001c0003t0002g0334others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-1620_364-1619d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | ||||||
chr16:74729004
|
A | ATTT | 8 | a0001c0001t0003g0126a0001c0002t0003g0123a0001c0002t0003g0124others(5): Show | 8 | HG01192.hp1 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-1621_364-1619d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | ||||||
chr16:74729004
|
AT | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0061a0001c0001t0001g0093others(5): Show | 8 | HG01167.hp1 HG01975.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-1619delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | ||||||
chr16:74729005
|
T | A | 4 | a0001c0001t0001g0260a0001c0001t0003g0176a0001c0001t0003g0229others(1): Show | 4 | HG01074.hp1 HG01167.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1619A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729005 | ||||||
chr16:74729060
|
G | C | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1674C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729060 | ||||||
chr16:74729074
|
G | C | 1 | a0001c0004t0006g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364-1688C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729074 | ||||||
chr16:74729171
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 69 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.364-1785G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729171 | ||||||
chr16:74729221
|
G | A | 1 | a0001c0003t0003g0362 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.364-1835C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729221 | ||||||
chr16:74729277
|
G | A | 23 | a0001c0003t0001g0318a0001c0003t0002g0010a0001c0004t0004g0009others(20): Show | 25 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-1891C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729277 | ||||||
chr16:74729305
|
G | A | 1 | a0001c0002t0002g0292 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.364-1919C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729305 | ||||||
chr16:74729670
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.364-2284C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729670 | ||||||
chr16:74729846
|
G | C | 1 | a0001c0003t0002g0010 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.364-2460C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729846 | ||||||
chr16:74729854
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.364-2468C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729854 | ||||||
chr16:74729967
|
G | C | 15 | a0001c0001t0005g0188a0001c0003t0003g0329a0001c0003t0005g0305others(12): Show | 15 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-2581C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729967 | ||||||
chr16:74729986
|
A | C | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-2600T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729986 | ||||||
chr16:74730142
|
C | T | 1 | a0001c0003t0002g0334 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.364-2756G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730142 | ||||||
chr16:74730198
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.364-2812G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730198 | ||||||
chr16:74730233
|
A | T | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.364-2847T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730233 | ||||||
chr16:74730535
|
G | C | 4 | a0001c0002t0003g0123a0001c0002t0003g0124a0001c0002t0003g0127others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-3149C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730535 | ||||||
chr16:74730542
|
A | AAC | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 97 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.364-3158_364-3157d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730542 | ||||||
chr16:74730679
|
T | G | 15 | a0001c0002t0003g0123a0001c0002t0003g0124a0001c0002t0003g0127others(12): Show | 15 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.364-3293A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730679 | ||||||
chr16:74730895
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 86 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.364-3509G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730895 | ||||||
chr16:74730932
|
C | T | 4 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-3546G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730932 | ||||||
chr16:74730991
|
G | A | 28 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0001g0359others(25): Show | 30 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.364-3605C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730991 | ||||||
chr16:74731156
|
A | AT | 17 | a0001c0001t0001g0042a0001c0001t0001g0074a0001c0001t0001g0128others(14): Show | 17 | HG01081.hp2 HG01515.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-3771dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731156 | ||||||
chr16:74731243
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-3857G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731243 | ||||||
chr16:74731257
|
C | CCTGAGTA others(1): Show |
77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 82 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.364-3879_364-3872d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731257 | ||||||
chr16:74731298
|
C | CT | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 83 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.364-3913dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731298 | ||||||
chr16:74731298
|
CT | C | 20 | a0001c0002t0001g0133a0001c0002t0001g0183a0001c0002t0003g0123others(17): Show | 21 | HG01256.hp2 HG01884.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-3913delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731298 | ||||||
chr16:74731391
|
G | A | 1 | a0001c0005t0001g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-4005C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731391 | ||||||
chr16:74731456
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.364-4070G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731456 | ||||||
chr16:74731498
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0271 | 2 | HG00609.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.364-4112C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731498 | ||||||
chr16:74731595
|
G | A | 173 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0030others(170): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.364-4209C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731595 | ||||||
chr16:74731715
|
C | T | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364-4329G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731715 | ||||||
chr16:74731765
|
C | T | 1 | a0001c0013t0001g0106 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.364-4379G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731765 | ||||||
chr16:74731925
|
T | C | 3 | a0001c0003t0003g0329a0001c0003t0005g0305a0001c0003t0005g0361 | 3 | HG02615.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.364-4539A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731925 | ||||||
chr16:74732206
|
C | A | 14 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(11): Show | 15 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.364-4820G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732206 | ||||||
chr16:74732279
|
G | A | 32 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0001g0359others(29): Show | 34 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.364-4893C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732279 | ||||||
chr16:74732444
|
CTTTTT | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0058others(7): Show | 11 | HG02165.hp1 NA18940.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-5063_364-5059d others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732444 | ||||||
chr16:74732450
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(68): Show | 75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.364-5064A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732450 | ||||||
chr16:74732451
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.364-5065A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732451 | ||||||
chr16:74732549
|
G | C | 4 | a0001c0003t0009g0353a0001c0003t0009g0354a0001c0008t0009g0372others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-5163C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732549 | ||||||
chr16:74732669
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364-5283G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732669 | ||||||
chr16:74733155
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.364-5769C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733155 | ||||||
chr16:74733170
|
T | C | 1 | a0001c0001t0018g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.364-5784A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733170 | ||||||
chr16:74733234
|
G | A | 1 | a0001c0014t0003g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364-5848C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733234 | ||||||
chr16:74733352
|
C | T | 1 | a0001c0003t0003g0351 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.364-5966G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733352 | ||||||
chr16:74733630
|
G | C | 1 | a0001c0007t0001g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.364-6244C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733630 | ||||||
chr16:74733644
|
A | T | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364-6258T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733644 | ||||||
chr16:74733658
|
G | A | 2 | a0001c0001t0003g0253a0001c0006t0002g0346 | 2 | HG01123.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.364-6272C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733658 | ||||||
chr16:74733824
|
C | T | 1 | a0001c0004t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.363+6199G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733824 | ||||||
chr16:74733835
|
T | A | 171 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(168): Show | 175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.363+6188A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733835 | ||||||
chr16:74733960
|
G | A | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+6063C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733960 | ||||||
chr16:74734025
|
C | T | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+5998G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734025 | ||||||
chr16:74734048
|
C | T | 1 | a0001c0002t0001g0181 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.363+5975G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734048 | ||||||
chr16:74734072
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.363+5951G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734072 | ||||||
chr16:74734085
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(54): Show | 62 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.363+5938C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734085 | ||||||
chr16:74734096
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+5927T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734096 | ||||||
chr16:74734156
|
G | A | 1 | a0001c0001t0003g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.363+5867C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734156 | ||||||
chr16:74734171
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.363+5852C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734171 | ||||||
chr16:74734238
|
G | T | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+5785C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734238 | ||||||
chr16:74734350
|
C | T | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+5673G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734350 | ||||||
chr16:74734395
|
G | A | 1 | a0001c0003t0001g0319 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363+5628C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734395 | ||||||
chr16:74734423
|
G | A | 1 | a0001c0001t0003g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+5600C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734423 | ||||||
chr16:74734458
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0042others(15): Show | 20 | HG02165.hp1 NA18940.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.363+5565C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734458 | ||||||
chr16:74734635
|
G | A | 3 | a0001c0002t0001g0122a0001c0002t0001g0133a0001c0002t0001g0196 | 3 | HG00642.hp1 HG00733.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.363+5388C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734635 | ||||||
chr16:74734732
|
T | A | 1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363+5291A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734732 | ||||||
chr16:74734914
|
G | T | 114 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0030others(111): Show | 116 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.363+5109C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734914 | ||||||
chr16:74734972
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.363+5051C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734972 | ||||||
chr16:74734978
|
G | A | 11 | a0001c0001t0001g0128a0001c0001t0002g0160a0001c0001t0005g0188others(8): Show | 11 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+5045C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734978 | ||||||
chr16:74735021
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.363+5002C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735021 | ||||||
chr16:74735186
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+4837C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735186 | ||||||
chr16:74735189
|
G | T | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+4834C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735189 | ||||||
chr16:74735333
|
G | A | 5 | a0001c0002t0001g0004a0001c0002t0001g0053a0001c0002t0001g0095others(2): Show | 6 | HG02155.hp1 NA18994.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+4690C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735333 | ||||||
chr16:74735382
|
C | G | 20 | a0001c0001t0003g0126a0001c0002t0003g0123a0001c0002t0003g0124others(17): Show | 21 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+4641G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735382 | ||||||
chr16:74735463
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.363+4560G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735463 | ||||||
chr16:74735792
|
C | T | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.363+4231G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735792 | ||||||
chr16:74735932
|
G | A | 1 | a0001c0003t0011g0363 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363+4091C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735932 | ||||||
chr16:74736058
|
CT | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(102): Show | 107 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.363+3964delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736058 | ||||||
chr16:74736201
|
C | T | 31 | a0001c0001t0001g0286a0001c0001t0003g0008a0001c0001t0003g0043others(28): Show | 33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.363+3822G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736201 | ||||||
chr16:74736393
|
A | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(368): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.363+3630T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736393 | ||||||
chr16:74736401
|
G | C | 1 | a0001c0003t0009g0353 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+3622C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736401 | ||||||
chr16:74736613
|
C | T | 9 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(6): Show | 10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+3410G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736613 | ||||||
chr16:74736761
|
C | G | 1 | a0001c0001t0001g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.363+3262G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736761 | ||||||
chr16:74736767
|
C | T | 1 | a0001c0003t0009g0353 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+3256G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736767 | ||||||
chr16:74736778
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.363+3245A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736778 | ||||||
chr16:74736807
|
T | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(76): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.363+3216A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736807 | ||||||
chr16:74736824
|
T | C | 10 | a0001c0001t0001g0128a0001c0001t0002g0160a0001c0001t0005g0188others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+3199A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736824 | ||||||
chr16:74737011
|
G | C | 2 | a0001c0001t0001g0115a0001c0002t0001g0113 | 2 | HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.363+3012C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737011 | ||||||
chr16:74737064
|
C | T | 1 | a0001c0002t0002g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+2959G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737064 | ||||||
chr16:74737085
|
C | T | 1 | a0001c0003t0001g0339 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.363+2938G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737085 | ||||||
chr16:74737130
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.363+2893G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737130 | ||||||
chr16:74737154
|
G | C | 2 | a0002c0009t0001g0213a0002c0009t0001g0215 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.363+2869C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737154 | ||||||
chr16:74737242
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.363+2781C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737242 | ||||||
chr16:74737266
|
G | A | 3 | a0001c0002t0001g0172a0001c0002t0001g0274a0001c0002t0006g0273 | 3 | HG02056.hp1 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.363+2757C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737266 | ||||||
chr16:74737441
|
A | G | 1 | a0001c0004t0006g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.363+2582T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737441 | ||||||
chr16:74737467
|
G | A | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.363+2556C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737467 | ||||||
chr16:74737469
|
G | A | 63 | a0001c0001t0001g0101a0001c0001t0001g0150a0001c0001t0001g0207others(60): Show | 67 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.363+2554C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737469 | ||||||
chr16:74737480
|
G | A | 1 | a0001c0003t0005g0369 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.363+2543C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737480 | ||||||
chr16:74737640
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.363+2383G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737640 | ||||||
chr16:74737642
|
C | G | 1 | a0001c0005t0012g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.363+2381G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737642 | ||||||
chr16:74737643
|
C | T | 1 | a0001c0002t0002g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+2380G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737643 | ||||||
chr16:74737685
|
G | C | 172 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(169): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.363+2338C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737685 | ||||||
chr16:74737762
|
GGCCT | G | 15 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(12): Show | 16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+2257_363+2260d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737762 | ||||||
chr16:74737776
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.363+2247G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737776 | ||||||
chr16:74737888
|
A | C | 1 | a0001c0001t0003g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+2135T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737888 | ||||||
chr16:74737946
|
G | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 184 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.363+2077C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737946 | ||||||
chr16:74738033
|
G | A | 15 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(12): Show | 16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1990C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738033 | ||||||
chr16:74738082
|
G | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0299a0001c0001t0001g0303 | 3 | HG00738.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.363+1941C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738082 | ||||||
chr16:74738348
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(52): Show | 59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.363+1675C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738348 | ||||||
chr16:74738429
|
G | A | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.363+1594C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738429 | ||||||
chr16:74738609
|
C | A | 1 | a0001c0001t0003g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+1414G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738609 | ||||||
chr16:74738725
|
C | T | 1 | a0001c0002t0001g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.363+1298G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738725 | ||||||
chr16:74738746
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0293a0001c0001t0001g0294others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1277G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738746 | ||||||
chr16:74738748
|
C | G | 5 | a0001c0001t0001g0090a0001c0001t0001g0293a0001c0001t0001g0294others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1275G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738748 | ||||||
chr16:74738752
|
CT | C | 15 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(12): Show | 16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1270delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738752 | ||||||
chr16:74738864
|
G | A | 3 | a0001c0002t0001g0089a0001c0002t0001g0116a0001c0002t0001g0203 | 3 | NA18960.hp1 NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.363+1159C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738864 | ||||||
chr16:74738900
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(115): Show | 120 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.363+1123G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738900 | ||||||
chr16:74738953
|
G | A | 15 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(12): Show | 16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1070C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738953 | ||||||
chr16:74739091
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(52): Show | 59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.363+932G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739091 | ||||||
chr16:74739332
|
C | T | 1 | a0001c0001t0003g0191 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.363+691G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739332 | ||||||
chr16:74739337
|
C | A | 1 | a0001c0002t0001g0015 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.363+686G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739337 | ||||||
chr16:74739338
|
TCCCTCCA others(6): Show |
T | 1 | a0001c0005t0001g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.363+672_363+684del others(13): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739338 | ||||||
chr16:74739372
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.363+651C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739372 | ||||||
chr16:74739408
|
C | A | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363+615G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739408 | ||||||
chr16:74739428
|
C | T | 1 | a0001c0005t0012g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.363+595G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739428 | ||||||
chr16:74739578
|
G | A | 1 | a0001c0008t0009g0373 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+445C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739578 | ||||||
chr16:74739874
|
G | A | 3 | a0001c0002t0003g0123a0001c0002t0003g0124a0001c0002t0003g0127 | 3 | HG02965.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.363+149C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739874 | ||||||
chr16:74739917
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0167 | 2 | NA18960.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.363+106A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739917 | ||||||
chr16:74740006
|
C | A | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363+17G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74740006 | ||||||
chr16:74740250
|
G | A | 1 | a0001c0001t0002g0007 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.271-135C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740250 | ||||||
chr16:74740481
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.271-366C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740481 | ||||||
chr16:74740521
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(116): Show | 121 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.271-406C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740521 | ||||||
chr16:74740534
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.271-419G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740534 | ||||||
chr16:74740584
|
A | T | 4 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-469T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740584 | ||||||
chr16:74740606
|
A | G | 354 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(351): Show | 367 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.271-491T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740606 | ||||||
chr16:74740620
|
A | AAAT | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(90): Show | 98 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.271-508_271-506dup others(3): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
A | AAATAAT | 28 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0001g0085others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.271-511_271-506dup others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
A | AAATAATA others(2): Show |
9 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0266others(6): Show | 10 | HG00099.hp2 HG01516.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-514_271-506dup others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
A | T | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-505T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
AAAT | A | 22 | a0001c0001t0001g0065a0001c0001t0001g0286a0001c0001t0003g0043others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.271-508_271-506del others(3): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
AAATAAT | A | 49 | a0001c0001t0001g0128a0001c0001t0001g0207a0001c0001t0001g0208others(46): Show | 51 | HG00621.hp2 HG00639.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.271-511_271-506del others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
AAATAATA others(2): Show |
A | 91 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(88): Show | 94 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.271-514_271-506del others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
AAATAATA others(5): Show |
A | 3 | a0001c0003t0002g0364a0001c0003t0005g0367a0001c0003t0011g0363 | 3 | HG02922.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271-517_271-506del others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740620
|
AAATAATA others(8): Show |
A | 5 | a0001c0001t0001g0170a0001c0001t0001g0247a0001c0002t0001g0274others(2): Show | 5 | HG01123.hp1 HG02056.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-520_271-506del others(15): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | ||||||
chr16:74740673
|
T | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(53): Show | 60 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.271-558A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740673 | ||||||
chr16:74740876
|
A | G | 7 | a0001c0001t0001g0026a0001c0007t0001g0035a0001c0007t0001g0036others(4): Show | 7 | HG02071.hp1 HG02155.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-761T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740876 | ||||||
chr16:74740991
|
G | A | 2 | a0002c0009t0012g0088a0002c0020t0017g0360 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.271-876C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740991 | ||||||
chr16:74741117
|
G | C | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.271-1002C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741117 | ||||||
chr16:74741140
|
G | A | 4 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1025C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741140 | ||||||
chr16:74741381
|
A | G | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-1266T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741381 | ||||||
chr16:74741519
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.271-1404G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741519 | ||||||
chr16:74741557
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.271-1442G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741557 | ||||||
chr16:74741773
|
A | AAT | 9 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0065others(6): Show | 12 | HG00280.hp1 HG00408.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1660_271-1659d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATAT | 17 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0061others(14): Show | 19 | HG00280.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.271-1662_271-1659d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATATAT | 3 | a0001c0001t0001g0060a0001c0001t0003g0044a0001c0003t0001g0333 | 3 | HG02698.hp2 HG03942.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.271-1664_271-1659d others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATATATA others(1): Show |
16 | a0001c0001t0003g0126a0001c0001t0003g0244a0001c0001t0023g0296others(13): Show | 16 | HG00639.hp1 HG01074.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-1666_271-1659d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATATATA others(3): Show |
3 | a0001c0001t0003g0209a0001c0002t0015g0198a0001c0003t0001g0339 | 3 | HG02258.hp1 HG02683.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.271-1668_271-1659d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATATATA others(5): Show |
5 | a0001c0001t0001g0090a0001c0001t0001g0293a0001c0004t0007g0082others(2): Show | 5 | HG01069.hp2 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-1670_271-1659d others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATATATA others(7): Show |
4 | a0001c0001t0001g0299a0001c0003t0001g0318a0001c0003t0002g0340others(1): Show | 4 | HG00099.hp2 HG01257.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1672_271-1659d others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | AATATATA others(9): Show |
1 | a0001c0003t0001g0308 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.271-1674_271-1659d others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.271-1659_271-1658i others(17): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
A | T | 1 | a0001c0013t0001g0106 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.271-1658T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
AAT | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(17): Show | 20 | HG01975.hp1 HG01978.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-1660_271-1659d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
AATAT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0068a0001c0003t0003g0011others(2): Show | 7 | HG01358.hp1 HG02074.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-1662_271-1659d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741773
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0006g0289 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.271-1668_271-1659d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | ||||||
chr16:74741796
|
ATATATAT others(7): Show |
A | 1 | a0001c0004t0007g0100 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-1695_271-1682d others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741796 | ||||||
chr16:74741800
|
ATATATAT others(5): Show |
A | 1 | a0001c0007t0001g0141 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.271-1697_271-1686d others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741800 | ||||||
chr16:74741800
|
ATATATAT others(7): Show |
A | 6 | a0001c0003t0001g0320a0001c0003t0001g0321a0001c0003t0001g0322others(3): Show | 6 | HG02280.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-1699_271-1686d others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741800 | ||||||
chr16:74741802
|
ATATATAT others(3): Show |
A | 1 | a0001c0003t0001g0359 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.271-1697_271-1688d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741802 | ||||||
chr16:74741802
|
ATATATAT others(5): Show |
A | 25 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0051others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.271-1699_271-1688d others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741802 | ||||||
chr16:74741804
|
A | ATG | 6 | a0001c0001t0002g0005a0001c0002t0001g0116a0001c0002t0001g0203others(3): Show | 7 | HG01358.hp2 HG01496.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-1690_271-1689i others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | ||||||
chr16:74741804
|
A | ATGTG | 8 | a0001c0001t0001g0170a0001c0002t0001g0028a0001c0002t0001g0105others(5): Show | 8 | HG01123.hp1 HG01361.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-1690_271-1689i others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | ||||||
chr16:74741804
|
A | G | 4 | a0001c0001t0002g0177a0001c0002t0001g0089a0001c0002t0001g0120others(1): Show | 4 | HG02735.hp1 HG03041.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1689T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | ||||||
chr16:74741804
|
ATATATGT others(1): Show |
A | 4 | a0001c0001t0001g0237a0001c0001t0003g0232a0001c0001t0018g0272others(1): Show | 4 | HG01071.hp1 HG03239.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1697_271-1690d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | ||||||
chr16:74741804
|
ATATATGT others(3): Show |
A | 14 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0058others(11): Show | 15 | HG01109.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-1699_271-1690d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | ||||||
chr16:74741806
|
A | ATG | 5 | a0001c0001t0002g0180a0001c0002t0001g0112a0001c0002t0001g0113others(2): Show | 5 | HG00544.hp1 HG01123.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-1692_271-1691i others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | ||||||
chr16:74741806
|
A | ATGTG | 25 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0260others(22): Show | 25 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.271-1692_271-1691i others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | ||||||
chr16:74741806
|
A | ATGTGTG | 4 | a0001c0001t0003g0229a0001c0002t0001g0154a0001c0002t0001g0172others(1): Show | 4 | HG01934.hp1 HG03017.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1692_271-1691i others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | ||||||
chr16:74741806
|
A | G | 22 | a0001c0001t0001g0170a0001c0001t0002g0005a0001c0001t0002g0177others(19): Show | 23 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.271-1691T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | ||||||
chr16:74741808
|
A | ATATATAT others(19): Show |
1 | a0001c0004t0001g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(28): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0303 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(21): Show |
1 | a0001c0002t0001g0196 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(30): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0003g0202a0001c0019t0016g0366 | 2 | HG01884.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(13): Show |
1 | a0001c0005t0010g0325 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(22): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(11): Show |
1 | a0001c0005t0012g0368 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0282a0001c0003t0002g0010 | 3 | HG00738.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(22): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(15): Show |
2 | a0001c0002t0001g0144a0001c0003t0003g0351 | 2 | HG02738.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(17): Show |
1 | a0001c0006t0002g0347 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0156a0001c0002t0001g0146 | 2 | HG00642.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0005g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(17): Show |
1 | a0001c0003t0005g0370 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(7): Show |
2 | a0002c0016t0001g0214a0002c0017t0021g0021 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(9): Show |
1 | a0001c0006t0002g0342 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0030g0157a0001c0003t0005g0369a0001c0004t0004g0279others(2): Show | 5 | HG00323.hp1 HG00735.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0024g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0128a0003c0021t0001g0374 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(9): Show |
1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0207a0001c0003t0005g0367 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(3): Show |
7 | a0001c0001t0001g0283a0001c0001t0001g0287a0001c0001t0001g0294others(4): Show | 7 | HG02698.hp1 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1694_271-1693i others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0150a0001c0002t0001g0122 | 2 | HG00642.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(7): Show |
2 | a0001c0003t0003g0338a0001c0008t0027g0348 | 2 | HG01256.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0208 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATAT others(5): Show |
2 | a0001c0002t0001g0145a0001c0002t0001g0173 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATATGT others(3): Show |
2 | a0001c0001t0001g0147a0001c0004t0019g0281 | 2 | HG02486.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATGTG | 3 | a0001c0001t0001g0153a0001c0001t0003g0275a0001c0002t0001g0178 | 3 | HG02155.hp1 HG03209.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATATGTGT others(1): Show |
12 | a0001c0001t0001g0102a0001c0001t0001g0151a0001c0001t0001g0152others(9): Show | 13 | HG01952.hp2 HG01975.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.271-1694_271-1693i others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATGTG | 5 | a0001c0001t0001g0091a0001c0002t0001g0004a0001c0002t0001g0095others(2): Show | 6 | NA18960.hp2 NA18963.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-1697_271-1694d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATGTGTG | 17 | a0001c0001t0001g0148a0001c0001t0001g0205a0001c0001t0002g0162others(14): Show | 18 | HG00099.hp1 HG00140.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-1699_271-1694d others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | ATGTGTGT others(1): Show |
4 | a0001c0001t0002g0047a0001c0002t0001g0048a0001c0002t0008g0171others(1): Show | 4 | HG02486.hp2 NA18612.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1701_271-1694d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741808
|
A | G | 81 | a0001c0001t0001g0056a0001c0001t0001g0066a0001c0001t0001g0070others(78): Show | 83 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.271-1693T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | ||||||
chr16:74741810
|
G | A | 40 | a0001c0001t0001g0049a0001c0001t0001g0137a0001c0001t0001g0201others(37): Show | 40 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.271-1695C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741810 | ||||||
chr16:74741812
|
G | A | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.271-1697C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741812 | ||||||
chr16:74741814
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0266a0001c0001t0001g0267others(4): Show | 7 | HG00609.hp2 HG02451.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1699C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741814 | ||||||
chr16:74741816
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-1701C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741816 | ||||||
chr16:74741818
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-1703C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741818 | ||||||
chr16:74741828
|
GTGTGTGT others(4): Show |
G | 16 | a0001c0001t0001g0056a0001c0001t0001g0134a0001c0001t0001g0193others(13): Show | 16 | HG00735.hp1 HG01192.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.271-1724_271-1714d others(13): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741828 | ||||||
chr16:74741829
|
T | C | 2 | a0001c0001t0002g0156a0001c0001t0030g0157 | 2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-1714A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741829 | ||||||
chr16:74741830
|
GTGTGTGT others(2): Show |
G | 29 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0040others(26): Show | 30 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.271-1724_271-1716d others(11): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741830 | ||||||
chr16:74741832
|
GTGTGTAT | G | 10 | a0001c0001t0001g0049a0001c0001t0001g0137a0001c0001t0001g0234others(7): Show | 10 | HG01081.hp1 HG02132.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-1724_271-1718d others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741832 | ||||||
chr16:74741834
|
GTGTAT | G | 10 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0002g0031others(7): Show | 10 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1724_271-1720d others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741834 | ||||||
chr16:74741836
|
GTAT | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0032others(52): Show | 56 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.271-1724_271-1722d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741836 | ||||||
chr16:74741838
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-1723T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741838 | ||||||
chr16:74741862
|
G | GTGTA | 3 | a0001c0001t0001g0128a0001c0001t0002g0160a0003c0021t0001g0374 | 3 | HG03098.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.271-1748_271-1747i others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741862 | ||||||
chr16:74742126
|
A | G | 1 | a0001c0002t0002g0292 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.271-2011T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742126 | ||||||
chr16:74742166
|
C | A | 1 | a0001c0001t0030g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.271-2051G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742166 | ||||||
chr16:74742239
|
C | T | 4 | a0001c0003t0009g0353a0001c0003t0009g0354a0001c0008t0009g0372others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2124G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742239 | ||||||
chr16:74742273
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 200 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.271-2158C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742273 | ||||||
chr16:74742364
|
C | T | 9 | a0001c0001t0001g0090a0001c0001t0001g0128a0001c0001t0002g0160others(6): Show | 9 | HG02622.hp1 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-2249G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742364 | ||||||
chr16:74742438
|
A | T | 1 | a0001c0005t0004g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.271-2323T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742438 | ||||||
chr16:74742532
|
G | T | 1 | a0001c0001t0002g0131 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.271-2417C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742532 | ||||||
chr16:74742730
|
C | T | 4 | a0001c0001t0005g0188a0001c0003t0005g0367a0001c0003t0005g0369others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2615G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742730 | ||||||
chr16:74742944
|
T | C | 1 | a0001c0002t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.271-2829A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742944 | ||||||
chr16:74743183
|
A | G | 1 | a0001c0001t0028g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.271-3068T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743183 | ||||||
chr16:74743194
|
A | T | 2 | a0001c0003t0001g0328a0001c0003t0002g0327 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3079T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743194 | ||||||
chr16:74743431
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.271-3316G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743431 | ||||||
chr16:74743498
|
T | C | 2 | a0001c0001t0002g0156a0001c0001t0030g0157 | 2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-3383A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743498 | ||||||
chr16:74743540
|
T | G | 4 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0002g0295others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3425A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743540 | ||||||
chr16:74743569
|
A | C | 4 | a0001c0003t0009g0353a0001c0003t0009g0354a0001c0008t0009g0372others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3454T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743569 | ||||||
chr16:74743650
|
G | A | 2 | a0001c0001t0002g0156a0001c0001t0030g0157 | 2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-3535C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743650 | ||||||
chr16:74743700
|
G | T | 1 | a0001c0001t0003g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.271-3585C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743700 | ||||||
chr16:74743704
|
C | A | 1 | a0001c0001t0024g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.271-3589G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743704 | ||||||
chr16:74743805
|
C | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0190a0001c0001t0003g0191 | 4 | NA19009.hp2 NA19064.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3690G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743805 | ||||||
chr16:74743896
|
G | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(113): Show | 118 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.271-3781C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743896 | ||||||
chr16:74744027
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.271-3912G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744027 | ||||||
chr16:74744065
|
G | A | 2 | a0001c0003t0002g0364a0001c0003t0011g0363 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271-3950C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744065 | ||||||
chr16:74744108
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 201 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.271-3993C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744108 | ||||||
chr16:74744140
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.271-4025C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744140 | ||||||
chr16:74744232
|
T | C | 1 | a0001c0001t0011g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.271-4117A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744232 | ||||||
chr16:74744264
|
C | A | 16 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(13): Show | 17 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.271-4149G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744264 | ||||||
chr16:74744265
|
C | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(52): Show | 59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.271-4150G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744265 | ||||||
chr16:74744394
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.271-4279T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744394 | ||||||
chr16:74744450
|
C | CT | 12 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0075others(9): Show | 12 | HG01934.hp1 HG02074.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-4336dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744450 | ||||||
chr16:74744450
|
CT | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0032others(62): Show | 66 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.271-4336delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744450 | ||||||
chr16:74744450
|
CTT | C | 78 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0040others(75): Show | 79 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.271-4337_271-4336d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744450 | ||||||
chr16:74744530
|
C | T | 1 | a0001c0003t0002g0327 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271-4415G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744530 | ||||||
chr16:74744708
|
T | A | 3 | a0001c0001t0001g0032a0001c0001t0002g0251a0001c0001t0002g0252 | 3 | HG02015.hp1 NA18965.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.271-4593A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744708 | ||||||
chr16:74744877
|
C | T | 4 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4762G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744877 | ||||||
chr16:74744986
|
G | C | 4 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4871C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744986 | ||||||
chr16:74745012
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 35 | HG00621.hp1 HG01975.hp1 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.271-4897C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745012 | ||||||
chr16:74745072
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.271-4957A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745072 | ||||||
chr16:74745194
|
T | C | 2 | a0001c0005t0010g0325a0001c0005t0010g0326 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.271-5079A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745194 | ||||||
chr16:74745378
|
G | T | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-5263C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745378 | ||||||
chr16:74745485
|
C | T | 9 | a0001c0001t0001g0166a0001c0001t0002g0005a0001c0001t0002g0069others(6): Show | 10 | HG01358.hp2 HG01496.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-5370G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745485 | ||||||
chr16:74745517
|
C | A | 11 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(8): Show | 12 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-5402G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745517 | ||||||
chr16:74745577
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.271-5462T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745577 | ||||||
chr16:74745740
|
C | T | 1 | a0001c0004t0006g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.271-5625G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745740 | ||||||
chr16:74745799
|
A | AT | 14 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0059others(11): Show | 14 | HG01981.hp1 HG02145.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-5685dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745799 | ||||||
chr16:74745799
|
AT | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(273): Show | 288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.271-5685delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745799 | ||||||
chr16:74745799
|
ATT | A | 12 | a0001c0001t0001g0085a0001c0001t0001g0234a0001c0001t0001g0286others(9): Show | 12 | HG00140.hp2 HG01928.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-5686_271-5685d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745799 | ||||||
chr16:74745937
|
T | C | 149 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(146): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.271-5822A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745937 | ||||||
chr16:74746054
|
G | A | 146 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(143): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.271-5939C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746054 | ||||||
chr16:74746069
|
G | T | 2 | a0001c0001t0002g0156a0001c0001t0030g0157 | 2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-5954C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746069 | ||||||
chr16:74746372
|
A | AT | 6 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0063others(3): Show | 7 | NA19002.hp1 NA19007.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-6258dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746372 | ||||||
chr16:74746374
|
TA | T | 14 | a0001c0001t0001g0170a0001c0002t0001g0116a0001c0002t0002g0292others(11): Show | 15 | HG01069.hp1 HG01071.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-6260delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746374 | ||||||
chr16:74746375
|
A | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(47): Show | 51 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.271-6260T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746375 | ||||||
chr16:74746376
|
TTA | T | 14 | a0001c0001t0001g0286a0001c0001t0003g0043a0001c0001t0003g0044others(11): Show | 14 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-6263_271-6262d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746376 | ||||||
chr16:74746377
|
TA | T | 144 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0101others(141): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.271-6263delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746377 | ||||||
chr16:74746378
|
A | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(96): Show | 105 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.271-6263T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746378 | ||||||
chr16:74746516
|
G | A | 16 | a0001c0003t0001g0308a0001c0003t0001g0318a0001c0003t0002g0010others(13): Show | 17 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.271-6401C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746516 | ||||||
chr16:74746592
|
C | A | 11 | a0001c0001t0002g0047a0001c0001t0002g0251a0001c0001t0002g0252others(8): Show | 11 | HG00597.hp1 HG02015.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.271-6477G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746592 | ||||||
chr16:74746961
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(121): Show | 126 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.271-6846G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746961 | ||||||
chr16:74747184
|
A | T | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-7069T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747184 | ||||||
chr16:74747251
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.271-7136G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747251 | ||||||
chr16:74747331
|
TAAGA | T | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(373): Show |
intron_variant | MODIFIER | c.271-7220_271-7217d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747331 | ||||||
chr16:74747334
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.271-7219C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747334 | ||||||
chr16:74747335
|
A | T | 1 | a0001c0001t0003g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.271-7220T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747335 | ||||||
chr16:74747355
|
A | G | 1 | a0001c0004t0007g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.271-7240T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747355 | ||||||
chr16:74747419
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.271-7304C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747419 | ||||||
chr16:74747618
|
C | T | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.271-7503G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747618 | ||||||
chr16:74747619
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(291): Show | 304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.271-7504T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747619 | ||||||
chr16:74747896
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 122 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.271-7781G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747896 | ||||||
chr16:74748216
|
G | C | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(366): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.271-8101C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748216 | ||||||
chr16:74748254
|
C | T | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-8139G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748254 | ||||||
chr16:74748350
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.271-8235A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748350 | ||||||
chr16:74748542
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(63): Show | 71 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.271-8427C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748542 | ||||||
chr16:74748777
|
T | G | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.271-8662A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748777 | ||||||
chr16:74748793
|
G | A | 1 | a0005c0011t0020g0013 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.271-8678C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748793 | ||||||
chr16:74748956
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(34): Show | 39 | HG00621.hp1 HG01069.hp2 HG01975.hp1 others(36): Show |
intron_variant | MODIFIER | c.271-8841C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748956 | ||||||
chr16:74749160
|
G | C | 1 | a0001c0002t0001g0116 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.271-9045C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749160 | ||||||
chr16:74749372
|
C | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(168): Show | 176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.271-9257G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749372 | ||||||
chr16:74749393
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271-9278G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749393 | ||||||
chr16:74749462
|
G | A | 6 | a0001c0003t0003g0324a0001c0005t0004g0323a0001c0005t0010g0325others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-9347C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749462 | ||||||
chr16:74749467
|
C | A | 1 | a0001c0003t0001g0333 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.271-9352G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749467 | ||||||
chr16:74749500
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(112): Show | 118 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.271-9385T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749500 | ||||||
chr16:74749582
|
T | A | 58 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(55): Show | 60 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.271-9467A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749582 | ||||||
chr16:74749851
|
G | A | 8 | a0001c0001t0001g0303a0001c0001t0003g0276a0001c0003t0001g0359others(5): Show | 9 | HG02145.hp2 HG02922.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-9736C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749851 | ||||||
chr16:74749864
|
G | A | 1 | a0001c0001t0014g0033 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.271-9749C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749864 | ||||||
chr16:74749871
|
T | C | 2 | a0001c0008t0009g0372a0001c0008t0009g0373 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.271-9756A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749871 | ||||||
chr16:74750233
|
G | A | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-10118C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750233 | ||||||
chr16:74750271
|
G | A | 4 | a0001c0001t0003g0006a0001c0001t0003g0190a0001c0001t0003g0191others(1): Show | 5 | NA19009.hp2 NA19064.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-10156C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750271 | ||||||
chr16:74750421
|
T | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(26): Show | 33 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.271-10306A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750421 | ||||||
chr16:74750517
|
G | C | 1 | a0001c0001t0007g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.271-10402C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750517 | ||||||
chr16:74750551
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.271-10436C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750551 | ||||||
chr16:74750761
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0024a0001c0001t0001g0128a0001c0003t0002g0355others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-10654_271-1064 others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(3): Show |
12 | a0001c0001t0001g0023a0001c0001t0002g0160a0001c0003t0002g0364others(9): Show | 12 | HG01069.hp2 HG02886.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-10656_271-1064 others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(5): Show |
15 | a0001c0001t0001g0020a0001c0001t0001g0223a0001c0001t0001g0247others(12): Show | 15 | HG01071.hp1 HG01074.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-10658_271-1064 others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(7): Show |
58 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0026others(55): Show | 61 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.271-10660_271-1064 others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(9): Show |
58 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(55): Show | 61 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.271-10662_271-1064 others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(11): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0030others(45): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.271-10664_271-1064 others(22): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(13): Show |
11 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0299others(8): Show | 12 | HG00738.hp1 HG01358.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-10666_271-1064 others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.271-10668_271-1064 others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750761
|
CTG | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0102others(103): Show | 109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.271-10648_271-1064 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | ||||||
chr16:74750781
|
G | GTGTGTGT others(5): Show |
14 | a0001c0003t0001g0308a0001c0003t0001g0315a0001c0003t0001g0316others(11): Show | 15 | HG00099.hp2 HG01192.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.271-10667_271-1066 others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | ||||||
chr16:74750781
|
G | GTGTGTGT others(7): Show |
1 | a0001c0003t0001g0321 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.271-10667_271-1066 others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | ||||||
chr16:74750781
|
G | GTGTGTGT others(9): Show |
10 | a0001c0003t0001g0320a0001c0003t0001g0322a0001c0003t0003g0324others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-10667_271-1066 others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | ||||||
chr16:74750781
|
G | GTGTGTGT others(15): Show |
1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-10667_271-1066 others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | ||||||
chr16:74750790
|
T | C | 2 | a0001c0008t0009g0372a0001c0008t0009g0373 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.271-10675A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | ||||||
chr16:74750790
|
T | TGTGTGC | 5 | a0001c0003t0005g0369a0001c0003t0005g0370a0001c0003t0009g0353others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-10676_271-1067 others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | ||||||
chr16:74750790
|
T | TGTGTGTG others(3): Show |
1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-10676_271-1067 others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | ||||||
chr16:74750790
|
T | TGTGTGTG others(10): Show |
2 | a0001c0001t0003g0220a0001c0002t0002g0292 | 2 | HG01517.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.271-10676_271-1067 others(21): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | ||||||
chr16:74750790
|
T | TGTGTGTG others(13): Show |
1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-10676_271-1067 others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | ||||||
chr16:74750857
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-10742G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750857 | ||||||
chr16:74750937
|
A | G | 2 | a0001c0004t0004g0279a0001c0004t0004g0301 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.271-10822T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750937 | ||||||
chr16:74751129
|
C | T | 1 | a0001c0002t0003g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.271-11014G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751129 | ||||||
chr16:74751226
|
C | A | 3 | a0001c0001t0001g0303a0001c0001t0003g0276a0001c0003t0002g0352 | 3 | HG02922.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.271-11111G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751226 | ||||||
chr16:74751272
|
T | G | 1 | a0001c0002t0001g0144 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.271-11157A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751272 | ||||||
chr16:74751286
|
G | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0102others(99): Show | 105 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.271-11171C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751286 | ||||||
chr16:74751304
|
C | T | 1 | a0001c0002t0003g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.271-11189G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751304 | ||||||
chr16:74751428
|
C | T | 1 | a0001c0003t0003g0350 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.271-11313G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751428 | ||||||
chr16:74751500
|
C | A | 2 | a0001c0003t0005g0305a0001c0003t0005g0361 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.271-11385G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751500 | ||||||
chr16:74751679
|
C | CGGACAGC others(8): Show |
10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-11579_271-1156 others(19): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751679 | ||||||
chr16:74751888
|
G | C | 65 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.271-11773C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751888 | ||||||
chr16:74751932
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(26): Show | 30 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.271-11817C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751932 | ||||||
chr16:74752004
|
A | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(27): Show | 34 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.271-11889T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752004 | ||||||
chr16:74752134
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.271-12019G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752134 | ||||||
chr16:74752198
|
C | G | 3 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-12083G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752198 | ||||||
chr16:74752203
|
G | A | 62 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(59): Show | 64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12088C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752203 | ||||||
chr16:74752264
|
A | T | 62 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(59): Show | 64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12149T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752264 | ||||||
chr16:74752280
|
G | C | 62 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(59): Show | 64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12165C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752280 | ||||||
chr16:74752401
|
C | T | 1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-12286G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752401 | ||||||
chr16:74752475
|
G | T | 1 | a0001c0003t0009g0353 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.271-12360C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752475 | ||||||
chr16:74752513
|
A | T | 61 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(58): Show | 63 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.271-12398T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752513 | ||||||
chr16:74752550
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.271-12435A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752550 | ||||||
chr16:74752563
|
G | C | 36 | a0001c0001t0001g0101a0001c0001t0003g0202a0001c0001t0003g0217others(33): Show | 37 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.271-12448C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752563 | ||||||
chr16:74752595
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.271-12480G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752595 | ||||||
chr16:74752666
|
G | C | 2 | a0001c0001t0001g0250a0001c0001t0002g0249 | 2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.271-12551C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752666 | ||||||
chr16:74752718
|
G | A | 62 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0227others(59): Show | 64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12603C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752718 | ||||||
chr16:74753101
|
C | T | 30 | a0001c0001t0024g0022a0001c0003t0001g0308a0001c0003t0001g0315others(27): Show | 32 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.271-12986G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753101 | ||||||
chr16:74753349
|
C | T | 4 | a0001c0001t0002g0156a0001c0001t0003g0155a0001c0001t0003g0209others(1): Show | 4 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-13234G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753349 | ||||||
chr16:74753445
|
T | C | 2 | a0001c0001t0002g0251a0001c0001t0002g0252 | 2 | HG02015.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.271-13330A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753445 | ||||||
chr16:74753453
|
G | A | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.271-13338C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753453 | ||||||
chr16:74753456
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.271-13341A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753456 | ||||||
chr16:74753534
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 144 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.271-13419C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753534 | ||||||
chr16:74753654
|
C | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 144 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.271-13539G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753654 | ||||||
chr16:74753720
|
G | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(75): Show | 80 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-13605C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753720 | ||||||
chr16:74753777
|
G | A | 105 | a0001c0001t0001g0085a0001c0001t0001g0101a0001c0001t0001g0223others(102): Show | 109 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.271-13662C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753777 | ||||||
chr16:74753821
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.271-13706A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753821 | ||||||
chr16:74753941
|
G | A | 62 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0223others(59): Show | 64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-13826C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753941 | ||||||
chr16:74753954
|
T | C | 3 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-13839A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753954 | ||||||
chr16:74754087
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(31): Show | 35 | HG00621.hp1 HG01069.hp2 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.271-13972C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754087 | ||||||
chr16:74754108
|
T | C | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-13993A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754108 | ||||||
chr16:74754110
|
T | C | 7 | a0001c0003t0002g0355a0001c0003t0002g0356a0001c0003t0002g0357others(4): Show | 7 | HG01891.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-13995A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754110 | ||||||
chr16:74754134
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.271-14019C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754134 | ||||||
chr16:74754148
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.271-14033G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754148 | ||||||
chr16:74754201
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.271-14086C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754201 | ||||||
chr16:74754201
|
G | T | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-14086C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754201 | ||||||
chr16:74754255
|
G | C | 4 | a0001c0001t0001g0227a0001c0001t0003g0253a0001c0001t0003g0254others(1): Show | 4 | HG03710.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-14140C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754255 | ||||||
chr16:74754404
|
A | G | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-14289T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754404 | ||||||
chr16:74754431
|
T | A | 1 | a0001c0002t0001g0146 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-14316A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754431 | ||||||
chr16:74754433
|
T | C | 2 | a0001c0001t0003g0084a0001c0001t0003g0275 | 2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.271-14318A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754433 | ||||||
chr16:74754484
|
G | A | 26 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(23): Show | 27 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.271-14369C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754484 | ||||||
chr16:74754613
|
T | C | 1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-14498A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754613 | ||||||
chr16:74754739
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.271-14624C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754739 | ||||||
chr16:74754789
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.271-14674T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754789 | ||||||
chr16:74754853
|
A | G | 1 | a0001c0002t0002g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.271-14738T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754853 | ||||||
chr16:74754909
|
T | C | 32 | a0001c0001t0001g0303a0001c0001t0003g0276a0001c0003t0001g0308others(29): Show | 34 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.271-14794A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754909 | ||||||
chr16:74754916
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-14801T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754916 | ||||||
chr16:74755011
|
C | G | 1 | a0001c0004t0004g0210 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.271-14896G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755011 | ||||||
chr16:74755036
|
C | T | 3 | a0001c0003t0001g0359a0001c0008t0003g0358a0002c0020t0017g0360 | 3 | HG02145.hp2 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.271-14921G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755036 | ||||||
chr16:74755079
|
C | G | 2 | a0001c0001t0001g0001a0004c0015t0001g0302 | 5 | HG00280.hp1 HG01361.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-14964G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755079 | ||||||
chr16:74755120
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(15): Show | 21 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-15005G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755120 | ||||||
chr16:74755121
|
G | A | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-15006C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755121 | ||||||
chr16:74755159
|
G | GT | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(127): Show | 134 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.271-15045dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755159 | ||||||
chr16:74755159
|
G | GTT | 113 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0061others(110): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.271-15046_271-1504 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755159 | ||||||
chr16:74755180
|
G | A | 1 | a0001c0002t0001g0146 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-15065C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755180 | ||||||
chr16:74755489
|
T | C | 1 | a0001c0001t0003g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.271-15374A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755489 | ||||||
chr16:74755568
|
A | C | 2 | a0001c0001t0024g0022a0002c0017t0021g0021 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.271-15453T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755568 | ||||||
chr16:74755878
|
T | TA | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(112): Show | 119 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.271-15764dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755878 | ||||||
chr16:74756158
|
G | C | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-16043C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756158 | ||||||
chr16:74756172
|
C | T | 2 | a0001c0003t0005g0305a0001c0003t0005g0361 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.271-16057G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756172 | ||||||
chr16:74756177
|
A | G | 1 | a0001c0002t0001g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.271-16062T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756177 | ||||||
chr16:74756202
|
C | T | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-16087G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756202 | ||||||
chr16:74756337
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-16222G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756337 | ||||||
chr16:74756386
|
T | C | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-16271A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756386 | ||||||
chr16:74756600
|
A | G | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-16485T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756600 | ||||||
chr16:74756644
|
T | C | 31 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(28): Show | 33 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.271-16529A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756644 | ||||||
chr16:74756678
|
A | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(98): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.271-16563T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756678 | ||||||
chr16:74756734
|
T | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0299 | 2 | HG00738.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.271-16619A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756734 | ||||||
chr16:74756760
|
A | G | 4 | a0001c0003t0001g0359a0001c0005t0013g0012a0001c0008t0003g0358others(1): Show | 5 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-16645T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756760 | ||||||
chr16:74756895
|
A | AAC | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(370): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.271-16782_271-1678 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756895 | ||||||
chr16:74756901
|
A | G | 9 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-16786T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756901 | ||||||
chr16:74757144
|
A | T | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-17029T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757144 | ||||||
chr16:74757172
|
A | G | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-17057T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757172 | ||||||
chr16:74757322
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.270+17164A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757322 | ||||||
chr16:74757402
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.270+17084A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757402 | ||||||
chr16:74757526
|
G | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.270+16960C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757526 | ||||||
chr16:74757616
|
T | C | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+16870A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757616 | ||||||
chr16:74757758
|
T | A | 3 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+16728A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757758 | ||||||
chr16:74757781
|
C | G | 1 | a0001c0004t0004g0210 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.270+16705G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757781 | ||||||
chr16:74757803
|
G | A | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+16683C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757803 | ||||||
chr16:74757871
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(78): Show | 83 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.270+16615A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757871 | ||||||
chr16:74757929
|
G | C | 27 | a0001c0003t0001g0308a0001c0003t0001g0315a0001c0003t0001g0316others(24): Show | 28 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.270+16557C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757929 | ||||||
chr16:74758091
|
G | A | 1 | a0001c0005t0001g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+16395C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758091 | ||||||
chr16:74758117
|
CT | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0086a0001c0001t0003g0043others(11): Show | 14 | HG01515.hp2 HG02486.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.270+16368delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758117 | ||||||
chr16:74758117
|
CTT | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 146 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.270+16367_270+1636 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758117 | ||||||
chr16:74758117
|
CTTT | C | 35 | a0001c0001t0001g0085a0001c0001t0001g0101a0001c0001t0003g0202others(32): Show | 36 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+16366_270+1636 others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758117 | ||||||
chr16:74758143
|
C | T | 57 | a0001c0001t0001g0223a0001c0001t0001g0227a0001c0001t0001g0230others(54): Show | 59 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.270+16343G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758143 | ||||||
chr16:74758160
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0271 | 2 | HG00609.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.270+16326C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758160 | ||||||
chr16:74758266
|
G | A | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.270+16220C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758266 | ||||||
chr16:74758280
|
C | T | 3 | a0001c0002t0001g0104a0001c0002t0008g0103a0001c0002t0029g0200 | 3 | NA18939.hp2 NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.270+16206G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758280 | ||||||
chr16:74758342
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+16144C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758342 | ||||||
chr16:74758345
|
C | T | 2 | a0001c0001t0024g0022a0002c0017t0021g0021 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.270+16141G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758345 | ||||||
chr16:74758440
|
C | T | 8 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+16046G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758440 | ||||||
chr16:74758553
|
A | C | 7 | a0001c0003t0002g0355a0001c0003t0002g0356a0001c0003t0002g0357others(4): Show | 7 | HG01891.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+15933T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758553 | ||||||
chr16:74758562
|
G | A | 2 | a0001c0003t0005g0305a0001c0003t0005g0361 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.270+15924C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758562 | ||||||
chr16:74758575
|
C | CT | 4 | a0001c0003t0001g0359a0001c0005t0013g0012a0001c0008t0003g0358others(1): Show | 5 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+15910dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758575 | ||||||
chr16:74758655
|
G | A | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+15831C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758655 | ||||||
chr16:74758723
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.270+15763G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758723 | ||||||
chr16:74758784
|
A | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(57): Show | 65 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.270+15702T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758784 | ||||||
chr16:74758912
|
G | A | 1 | a0002c0009t0012g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.270+15574C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758912 | ||||||
chr16:74758961
|
A | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.270+15525T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758961 | ||||||
chr16:74759159
|
G | C | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+15327C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759159 | ||||||
chr16:74759383
|
G | C | 1 | a0001c0002t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.270+15103C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759383 | ||||||
chr16:74759746
|
T | C | 8 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0293others(5): Show | 8 | HG00738.hp1 HG01891.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+14740A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759746 | ||||||
chr16:74759778
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.270+14708G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759778 | ||||||
chr16:74759796
|
T | G | 3 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+14690A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759796 | ||||||
chr16:74759818
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.270+14668G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759818 | ||||||
chr16:74759993
|
G | A | 5 | a0001c0003t0001g0315a0001c0003t0001g0316a0001c0003t0001g0317others(2): Show | 5 | HG02040.hp2 NA18966.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+14493C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759993 | ||||||
chr16:74760155
|
T | C | 1 | a0001c0005t0001g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+14331A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760155 | ||||||
chr16:74760157
|
C | T | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+14329G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760157 | ||||||
chr16:74760167
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0019others(35): Show | 40 | HG00621.hp1 HG01069.hp2 HG01975.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+14319G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760167 | ||||||
chr16:74760350
|
C | A | 8 | a0001c0004t0004g0009a0001c0004t0004g0210a0001c0004t0004g0279others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+14136G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760350 | ||||||
chr16:74760393
|
A | G | 1 | a0001c0004t0001g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.270+14093T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760393 | ||||||
chr16:74760420
|
G | A | 2 | a0001c0003t0001g0359a0001c0008t0003g0358 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+14066C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760420 | ||||||
chr16:74760567
|
T | A | 2 | a0001c0001t0003g0276a0001c0003t0002g0352 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.270+13919A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760567 | ||||||
chr16:74760573
|
G | A | 30 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(27): Show | 31 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.270+13913C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760573 | ||||||
chr16:74760599
|
C | T | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+13887G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760599 | ||||||
chr16:74760600
|
C | CA | 58 | a0001c0001t0001g0223a0001c0001t0001g0227a0001c0001t0001g0230others(55): Show | 60 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.270+13885dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760600 | ||||||
chr16:74760610
|
C | G | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270+13876G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760610 | ||||||
chr16:74760666
|
T | A | 9 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+13820A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760666 | ||||||
chr16:74760853
|
T | C | 1 | a0001c0002t0001g0117 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.270+13633A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760853 | ||||||
chr16:74761174
|
G | A | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+13312C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761174 | ||||||
chr16:74761367
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.270+13119G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761367 | ||||||
chr16:74761368
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+13118C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761368 | ||||||
chr16:74761452
|
CA | C | 7 | a0001c0003t0002g0355a0001c0003t0002g0356a0001c0003t0002g0357others(4): Show | 7 | HG01891.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+13033delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761452 | ||||||
chr16:74761458
|
A | AAAAG | 9 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+13024_270+1302 others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761458 | ||||||
chr16:74761458
|
AAAAG | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(174): Show | 183 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.270+13024_270+1302 others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761458 | ||||||
chr16:74761458
|
AAAAGAAA others(9): Show |
A | 59 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(56): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.270+13012_270+1302 others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761458 | ||||||
chr16:74761461
|
AGAAAG | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0090others(1): Show | 4 | HG02622.hp1 HG03490.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+13020_270+1302 others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761461 | ||||||
chr16:74761466
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(174): Show | 183 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.270+13020C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761466 | ||||||
chr16:74761470
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.270+13016C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761470 | ||||||
chr16:74761492
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12994G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761492 | ||||||
chr16:74761622
|
T | C | 2 | a0001c0003t0003g0350a0001c0003t0003g0351 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.270+12864A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761622 | ||||||
chr16:74761805
|
A | T | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+12681T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761805 | ||||||
chr16:74761909
|
C | T | 30 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(27): Show | 31 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.270+12577G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761909 | ||||||
chr16:74761956
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.270+12530G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761956 | ||||||
chr16:74761971
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.270+12515C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761971 | ||||||
chr16:74762058
|
T | A | 2 | a0001c0008t0009g0372a0001c0008t0009g0373 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+12428A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762058 | ||||||
chr16:74762076
|
A | ACT | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12408_270+1240 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762076 | ||||||
chr16:74762174
|
G | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12312C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762174 | ||||||
chr16:74762175
|
T | C | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+12311A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762175 | ||||||
chr16:74762234
|
G | A | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+12252C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762234 | ||||||
chr16:74762264
|
C | T | 27 | a0001c0003t0001g0308a0001c0003t0001g0315a0001c0003t0001g0316others(24): Show | 28 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.270+12222G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762264 | ||||||
chr16:74762290
|
G | A | 4 | a0001c0001t0003g0006a0001c0001t0003g0190a0001c0001t0003g0191others(1): Show | 5 | NA19009.hp2 NA19064.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+12196C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762290 | ||||||
chr16:74762323
|
G | A | 2 | a0001c0003t0009g0353a0001c0003t0009g0354 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.270+12163C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762323 | ||||||
chr16:74762333
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(74): Show | 79 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+12153C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762333 | ||||||
chr16:74762388
|
C | T | 2 | a0001c0001t0001g0027a0001c0002t0001g0028 | 2 | NA18972.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.270+12098G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762388 | ||||||
chr16:74762410
|
A | C | 1 | a0001c0003t0002g0334 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.270+12076T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762410 | ||||||
chr16:74762436
|
A | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12050T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762436 | ||||||
chr16:74762534
|
G | C | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+11952C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762534 | ||||||
chr16:74762617
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.270+11869C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762617 | ||||||
chr16:74762617
|
G | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+11869C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762617 | ||||||
chr16:74762692
|
G | A | 1 | a0001c0005t0010g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.270+11794C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762692 | ||||||
chr16:74762732
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11754T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762732 | ||||||
chr16:74762820
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11666T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762820 | ||||||
chr16:74762838
|
A | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.270+11648T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762838 | ||||||
chr16:74762844
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG02165.hp1 NA18994.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+11642T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762844 | ||||||
chr16:74762860
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.270+11626T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762860 | ||||||
chr16:74762864
|
G | C | 1 | a0001c0001t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.270+11622C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762864 | ||||||
chr16:74762936
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(77): Show | 82 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+11550C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762936 | ||||||
chr16:74763095
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11391C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763095 | ||||||
chr16:74763239
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11247T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763239 | ||||||
chr16:74763268
|
T | C | 1 | a0001c0002t0001g0274 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+11218A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763268 | ||||||
chr16:74763278
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.270+11208C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763278 | ||||||
chr16:74763383
|
G | C | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+11103C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763383 | ||||||
chr16:74763404
|
C | G | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+11082G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763404 | ||||||
chr16:74763405
|
G | T | 20 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(17): Show | 20 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.270+11081C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763405 | ||||||
chr16:74763414
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(25): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.270+11072G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763414 | ||||||
chr16:74763418
|
C | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0032others(14): Show | 17 | HG00621.hp2 HG00639.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+11068G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763418 | ||||||
chr16:74763446
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(90): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.270+11040G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763446 | ||||||
chr16:74763494
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.270+10992C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763494 | ||||||
chr16:74763496
|
G | A | 10 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+10990C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763496 | ||||||
chr16:74763500
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.270+10986G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763500 | ||||||
chr16:74763584
|
T | C | 3 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+10902A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763584 | ||||||
chr16:74763689
|
C | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(77): Show | 82 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+10797G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763689 | ||||||
chr16:74763701
|
A | T | 21 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(18): Show | 21 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+10785T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763701 | ||||||
chr16:74763708
|
T | TC | 93 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(90): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.270+10777dupG | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763708 | ||||||
chr16:74763746
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+10740C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763746 | ||||||
chr16:74763786
|
C | G | 2 | a0001c0001t0024g0022a0002c0017t0021g0021 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.270+10700G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763786 | ||||||
chr16:74763904
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0282others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+10582T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763904 | ||||||
chr16:74763982
|
T | C | 1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270+10504A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763982 | ||||||
chr16:74763983
|
T | C | 26 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(23): Show | 27 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.270+10503A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763983 | ||||||
chr16:74764075
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.270+10411A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764075 | ||||||
chr16:74764399
|
C | T | 1 | a0001c0002t0001g0130 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.270+10087G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764399 | ||||||
chr16:74764400
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.270+10086C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764400 | ||||||
chr16:74764428
|
T | C | 1 | a0001c0004t0025g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+10058A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764428 | ||||||
chr16:74764666
|
C | T | 3 | a0001c0008t0009g0372a0001c0008t0009g0373a0001c0019t0016g0366 | 3 | HG01884.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+9820G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764666 | ||||||
chr16:74764667
|
C | T | 1 | a0001c0002t0001g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.270+9819G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764667 | ||||||
chr16:74764726
|
T | TA | 33 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(30): Show | 35 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+9759dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764726 | ||||||
chr16:74764832
|
A | T | 3 | a0001c0001t0001g0128a0001c0012t0001g0014a0001c0014t0003g0129 | 3 | HG02109.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.270+9654T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764832 | ||||||
chr16:74764896
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(79): Show | 84 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.270+9590A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764896 | ||||||
chr16:74764986
|
C | T | 2 | a0001c0003t0001g0359a0001c0008t0003g0358 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+9500G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764986 | ||||||
chr16:74765022
|
G | A | 2 | a0001c0003t0001g0318a0001c0003t0002g0010 | 3 | HG00099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.270+9464C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765022 | ||||||
chr16:74765159
|
C | CT | 93 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(90): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.270+9326dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765159 | ||||||
chr16:74765159
|
CT | C | 59 | a0001c0001t0001g0223a0001c0001t0001g0227a0001c0001t0001g0230others(56): Show | 61 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.270+9326delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765159 | ||||||
chr16:74765220
|
G | A | 1 | a0001c0003t0001g0319 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.270+9266C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765220 | ||||||
chr16:74765242
|
C | T | 1 | a0001c0002t0003g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.270+9244G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765242 | ||||||
chr16:74765305
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(25): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.270+9181G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765305 | ||||||
chr16:74765306
|
G | A | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(366): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.270+9180C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765306 | ||||||
chr16:74765601
|
C | G | 1 | a0001c0001t0001g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+8885G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765601 | ||||||
chr16:74765613
|
C | A | 6 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+8873G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765613 | ||||||
chr16:74765638
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.270+8848C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765638 | ||||||
chr16:74765992
|
A | G | 1 | a0001c0005t0013g0012 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.270+8494T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765992 | ||||||
chr16:74766050
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0027others(34): Show | 37 | HG00621.hp2 HG00639.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.270+8436C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766050 | ||||||
chr16:74766149
|
A | G | 1 | a0001c0004t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.270+8337T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766149 | ||||||
chr16:74766151
|
T | A | 1 | a0001c0004t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.270+8335A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766151 | ||||||
chr16:74766476
|
A | C | 1 | a0001c0002t0003g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.270+8010T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766476 | ||||||
chr16:74766492
|
G | C | 1 | a0001c0002t0001g0258 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.270+7994C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766492 | ||||||
chr16:74766556
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(56): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.270+7930G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766556 | ||||||
chr16:74766588
|
A | C | 9 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+7898T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766588 | ||||||
chr16:74766642
|
AG | A | 45 | a0001c0001t0001g0101a0001c0001t0003g0276a0001c0003t0001g0308others(42): Show | 47 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.270+7843delC | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766642 | ||||||
chr16:74766651
|
G | T | 1 | a0001c0005t0001g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+7835C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766651 | ||||||
chr16:74766673
|
T | C | 3 | a0001c0003t0001g0359a0001c0008t0003g0358a0002c0020t0017g0360 | 3 | HG02145.hp2 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+7813A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766673 | ||||||
chr16:74766810
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.270+7676G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766810 | ||||||
chr16:74766819
|
A | G | 4 | a0001c0001t0001g0201a0001c0002t0001g0122a0001c0002t0001g0196others(1): Show | 4 | HG00642.hp1 HG00733.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+7667T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766819 | ||||||
chr16:74766915
|
G | A | 3 | a0001c0003t0001g0359a0001c0008t0003g0358a0002c0020t0017g0360 | 3 | HG02145.hp2 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+7571C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766915 | ||||||
chr16:74767185
|
T | G | 9 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+7301A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767185 | ||||||
chr16:74767257
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.270+7229G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767257 | ||||||
chr16:74767262
|
T | C | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270+7224A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767262 | ||||||
chr16:74767282
|
C | G | 2 | a0001c0001t0001g0101a0001c0003t0005g0371 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.270+7204G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767282 | ||||||
chr16:74767318
|
C | A | 2 | a0001c0005t0010g0330a0001c0005t0010g0331 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270+7168G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767318 | ||||||
chr16:74767412
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.270+7074T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767412 | ||||||
chr16:74767421
|
G | A | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+7065C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767421 | ||||||
chr16:74767442
|
C | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0027others(34): Show | 37 | HG00621.hp2 HG00639.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.270+7044G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767442 | ||||||
chr16:74767539
|
C | T | 1 | a0001c0001t0008g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.270+6947G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767539 | ||||||
chr16:74767717
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(75): Show | 80 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.270+6769C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767717 | ||||||
chr16:74767882
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.270+6604C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767882 | ||||||
chr16:74767883
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.270+6603A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767883 | ||||||
chr16:74767924
|
C | T | 1 | a0001c0004t0006g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+6562G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767924 | ||||||
chr16:74767976
|
G | A | 1 | a0001c0003t0005g0370 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.270+6510C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767976 | ||||||
chr16:74768013
|
A | G | 79 | a0001c0001t0001g0101a0001c0001t0003g0202a0001c0001t0003g0217others(76): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+6473T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768013 | ||||||
chr16:74768517
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.270+5969G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768517 | ||||||
chr16:74768523
|
A | C | 23 | a0001c0001t0001g0115a0001c0002t0001g0089a0001c0002t0001g0104others(20): Show | 23 | HG00544.hp1 HG02071.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.270+5963T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768523 | ||||||
chr16:74768588
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0003g0259 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.270+5898C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768588 | ||||||
chr16:74768622
|
A | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(77): Show | 82 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+5864T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768622 | ||||||
chr16:74768693
|
C | T | 27 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(24): Show | 28 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.270+5793G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768693 | ||||||
chr16:74768950
|
T | C | 9 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+5536A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768950 | ||||||
chr16:74768974
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+5512G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768974 | ||||||
chr16:74769008
|
G | A | 3 | a0001c0001t0001g0201a0001c0002t0001g0196a0001c0002t0001g0197 | 3 | HG00733.hp1 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.270+5478C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769008 | ||||||
chr16:74769028
|
C | T | 16 | a0001c0003t0001g0308a0001c0003t0001g0315a0001c0003t0001g0316others(13): Show | 17 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+5458G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769028 | ||||||
chr16:74769047
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.270+5439C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769047 | ||||||
chr16:74769154
|
A | G | 2 | a0001c0008t0009g0372a0001c0008t0009g0373 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+5332T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769154 | ||||||
chr16:74769177
|
C | T | 32 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(29): Show | 34 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+5309G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769177 | ||||||
chr16:74769180
|
C | G | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+5306G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769180 | ||||||
chr16:74769430
|
A | T | 1 | a0001c0002t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.270+5056T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769430 | ||||||
chr16:74769446
|
C | T | 8 | a0001c0003t0002g0355a0001c0003t0002g0356a0001c0003t0002g0357others(5): Show | 8 | HG01891.hp1 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+5040G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769446 | ||||||
chr16:74769492
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.270+4994A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769492 | ||||||
chr16:74769541
|
C | A | 9 | a0001c0001t0001g0101a0001c0003t0005g0367a0001c0003t0005g0369others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+4945G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769541 | ||||||
chr16:74769541
|
C | T | 1 | a0001c0005t0007g0332 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.270+4945G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769541 | ||||||
chr16:74769602
|
A | C | 32 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(29): Show | 33 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.270+4884T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769602 | ||||||
chr16:74769616
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.270+4870T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769616 | ||||||
chr16:74769628
|
C | T | 1 | a0001c0002t0015g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+4858G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769628 | ||||||
chr16:74769662
|
A | T | 1 | a0001c0003t0001g0333 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.270+4824T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769662 | ||||||
chr16:74769705
|
G | C | 1 | a0001c0004t0001g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.270+4781C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769705 | ||||||
chr16:74769729
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.270+4757T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769729 | ||||||
chr16:74769766
|
G | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(144): Show | 151 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.270+4720C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769766 | ||||||
chr16:74769826
|
G | C | 1 | a0001c0002t0001g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.270+4660C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769826 | ||||||
chr16:74769898
|
C | T | 1 | a0001c0001t0002g0005 | 2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.270+4588G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769898 | ||||||
chr16:74769969
|
G | A | 1 | a0001c0002t0029g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.270+4517C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769969 | ||||||
chr16:74770026
|
G | T | 1 | a0001c0004t0007g0100 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.270+4460C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770026 | ||||||
chr16:74770074
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.270+4412G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770074 | ||||||
chr16:74770157
|
A | C | 2 | a0001c0001t0024g0022a0002c0017t0021g0021 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.270+4329T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770157 | ||||||
chr16:74770312
|
G | C | 3 | a0001c0003t0001g0320a0001c0003t0001g0321a0001c0003t0001g0322 | 3 | HG02280.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.270+4174C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770312 | ||||||
chr16:74770374
|
T | G | 34 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(31): Show | 36 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+4112A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770374 | ||||||
chr16:74770374
|
T | TTTTG | 3 | a0002c0009t0001g0213a0002c0009t0001g0215a0002c0016t0001g0214 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+4108_270+4111d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770374 | ||||||
chr16:74770374
|
TTTTG | T | 4 | a0001c0003t0005g0367a0001c0003t0005g0369a0001c0003t0005g0370others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+4108_270+4111d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770374 | ||||||
chr16:74770441
|
G | A | 1 | a0002c0009t0012g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.270+4045C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770441 | ||||||
chr16:74770510
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0002g0222a0001c0001t0002g0224others(1): Show | 4 | HG01071.hp1 HG01109.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+3976G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770510 | ||||||
chr16:74770881
|
C | T | 2 | a0001c0002t0001g0094a0001c0002t0001g0098 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.270+3605G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770881 | ||||||
chr16:74770889
|
C | T | 4 | a0001c0003t0002g0364a0001c0003t0003g0362a0001c0003t0005g0361others(1): Show | 4 | HG02717.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+3597G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770889 | ||||||
chr16:74770951
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.270+3535G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770951 | ||||||
chr16:74771121
|
A | G | 9 | a0001c0003t0005g0367a0001c0003t0005g0369a0001c0003t0005g0370others(6): Show | 10 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+3365T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771121 | ||||||
chr16:74771230
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.270+3256T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771230 | ||||||
chr16:74771374
|
A | G | 2 | a0001c0002t0001g0004a0001c0002t0001g0095 | 3 | NA19066.hp1 NA19079.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.270+3112T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771374 | ||||||
chr16:74771626
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.270+2860C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771626 | ||||||
chr16:74771683
|
A | G | 1 | a0002c0020t0017g0360 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+2803T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771683 | ||||||
chr16:74771732
|
C | G | 76 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(73): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+2754G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771732 | ||||||
chr16:74771770
|
G | A | 76 | a0001c0001t0003g0202a0001c0001t0003g0217a0001c0001t0003g0218others(73): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+2716C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771770 | ||||||
chr16:74771778
|
C | T | 1 | a0001c0008t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270+2708G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771778 | ||||||
chr16:74771790
|
C | T | 34 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(31): Show | 36 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+2696G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771790 | ||||||
chr16:74771952
|
CT | C | 48 | a0001c0001t0001g0020a0001c0001t0001g0091a0001c0001t0001g0093others(45): Show | 50 | HG00099.hp1 HG00099.hp2 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.270+2533delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771952 | ||||||
chr16:74772012
|
G | A | 10 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+2474C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772012 | ||||||
chr16:74772043
|
C | T | 1 | a0001c0019t0016g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270+2443G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772043 | ||||||
chr16:74772146
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA18963.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.270+2340G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772146 | ||||||
chr16:74772231
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.270+2255C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772231 | ||||||
chr16:74772337
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.270+2149T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772337 | ||||||
chr16:74772345
|
C | G | 32 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(29): Show | 33 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.270+2141G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772345 | ||||||
chr16:74772346
|
T | C | 1 | a0001c0004t0004g0210 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.270+2140A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772346 | ||||||
chr16:74772360
|
C | G | 1 | a0001c0001t0001g0017 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.270+2126G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772360 | ||||||
chr16:74772375
|
C | G | 2 | a0001c0003t0005g0305a0001c0004t0004g0210 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.270+2111G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772375 | ||||||
chr16:74772386
|
T | C | 1 | a0001c0001t0018g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.270+2100A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772386 | ||||||
chr16:74772406
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+2080A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772406 | ||||||
chr16:74772470
|
C | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(217): Show | 227 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.270+2016G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772470 | ||||||
chr16:74772528
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+1958G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772528 | ||||||
chr16:74772721
|
T | G | 1 | a0001c0001t0001g0303 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270+1765A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772721 | ||||||
chr16:74772794
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.270+1692T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772794 | ||||||
chr16:74772871
|
T | C | 2 | a0001c0002t0001g0274a0001c0002t0006g0273 | 2 | HG02056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.270+1615A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772871 | ||||||
chr16:74773000
|
C | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.270+1486G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773000 | ||||||
chr16:74773110
|
G | C | 1 | a0001c0003t0002g0364 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.270+1376C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773110 | ||||||
chr16:74773114
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.270+1372C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773114 | ||||||
chr16:74773127
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+1359G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773127 | ||||||
chr16:74773165
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0223a0001c0001t0001g0227others(168): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.270+1321A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773165 | ||||||
chr16:74773241
|
A | C | 3 | a0001c0001t0003g0276a0001c0005t0001g0365a0001c0005t0013g0012 | 4 | HG03098.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+1245T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773241 | ||||||
chr16:74773315
|
C | A | 9 | a0001c0003t0001g0328a0001c0003t0002g0327a0001c0003t0003g0324others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+1171G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773315 | ||||||
chr16:74773351
|
AG | A | 64 | a0001c0001t0001g0223a0001c0001t0001g0227a0001c0001t0001g0230others(61): Show | 66 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.270+1134delC | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773351 | ||||||
chr16:74773594
|
C | T | 70 | a0001c0001t0003g0276a0001c0003t0001g0308a0001c0003t0001g0315others(67): Show | 73 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.270+892G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773594 | ||||||
chr16:74773635
|
T | C | 1 | a0001c0001t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.270+851A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773635 | ||||||
chr16:74773665
|
C | G | 29 | a0001c0003t0001g0308a0001c0003t0001g0315a0001c0003t0001g0316others(26): Show | 30 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.270+821G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773665 | ||||||
chr16:74773679
|
T | G | 3 | a0001c0001t0003g0276a0001c0005t0001g0365a0001c0005t0013g0012 | 4 | HG03098.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+807A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773679 | ||||||
chr16:74773682
|
G | C | 8 | a0001c0003t0005g0367a0001c0003t0005g0369a0001c0003t0005g0370others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+804C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773682 | ||||||
chr16:74773959
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0002g0277 | 2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.270+527C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773959 | ||||||
chr16:74774089
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0282a0001c0001t0001g0283others(25): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.270+397C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74774089 | ||||||
chr16:74774143
|
G | T | 1 | a0001c0002t0001g0015 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.270+343C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74774143 | ||||||
chr16:74774167
|
G | C | 1 | a0001c0002t0003g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.270+319C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74774167 |