geneid | 2153 |
---|---|
ensemblid | ENSG00000198734.12 |
hgncid | 3542 |
symbol | F5 |
name | coagulation factor V |
refseq_nuc | NM_000130.5 |
refseq_prot | NP_000121.2 |
ensembl_nuc | ENST00000367797.9 |
ensembl_prot | ENSP00000356771.3 |
mane_status | MANE Select |
chr | chr1 |
start | 169511951 |
end | 169586481 |
strand | - |
ver | v1.2 |
region | chr1:169511951-169586481 |
region5000 | chr1:169506951-169591481 |
regionname0 | F5_chr1_169511951_169586481 |
regionname5000 | F5_chr1_169506951_169591481 |
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 | 0/0 | 2224 | 63 | 0 | 4 | 54 | 0 | 5 | 42 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002 | 0/0 | 2224 | 39 | 7 | 15 | 8 | 4 | 5 | 8 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003 | 0/1 | 2224 | 37 | 4 | 8 | 15 | 0 | 9 | 11 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004 | 1/0 | 2224 | 30 | 11 | 6 | 0 | 6 | 6 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005 | 0/0 | 2224 | 30 | 4 | 10 | 12 | 1 | 3 | 6 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006 | 0/0 | 2224 | 19 | 0 | 8 | 8 | 1 | 2 | 8 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007 | 0/0 | 2224 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0008 | 0/0 | 2224 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0009 | 0/0 | 2224 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0010 | 0/0 | 2224 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0011 | 0/0 | 2224 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0012 | 0/0 | 2224 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0013 | 0/0 | 2224 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0014 | 0/0 | 2224 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0015 | 0/0 | 2224 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0016 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0017 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0018 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0019 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0020 | 0/0 | 2224 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0021 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0022 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0023 | 0/0 | 2224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0024 | 0/0 | 2224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0025 | 0/0 | 2224 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0026 | 0/0 | 2224 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0027 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0028 | 0/0 | 2224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0029 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0030 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0031 | 0/0 | 2224 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0032 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0033 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0034 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0035 | 0/0 | 2224 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0036 | 0/0 | 2224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0037 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0038 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0039 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0040 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0041 | 0/0 | 2224 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0042 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0043 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
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 | 0/0 | 6675 | 25 | 0 | 0 | 25 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0002 | 0/0 | 6675 | 25 | 0 | 3 | 18 | 0 | 4 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0003 | 0/0 | 6675 | 19 | 4 | 8 | 1 | 3 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0004 | 0/0 | 6675 | 12 | 0 | 1 | 10 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0005 | 0/0 | 6675 | 12 | 0 | 3 | 7 | 0 | 2 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0006 | 0/0 | 6675 | 10 | 2 | 1 | 6 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0007 | 0/0 | 6675 | 10 | 3 | 2 | 0 | 4 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0008 | 0/0 | 6675 | 10 | 0 | 6 | 3 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0009 | 0/0 | 6675 | 9 | 0 | 6 | 3 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0010 | 0/0 | 6675 | 9 | 1 | 5 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0011 | 0/0 | 6675 | 8 | 0 | 3 | 3 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0012 | 0/0 | 6675 | 7 | 5 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0013 | 0/0 | 6675 | 6 | 6 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0014 | 0/0 | 6675 | 6 | 0 | 0 | 6 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0015 | 0/0 | 6675 | 6 | 0 | 2 | 3 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0016 | 0/0 | 6675 | 5 | 3 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0017 | 0/0 | 6675 | 5 | 5 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0018 | 0/1 | 6675 | 5 | 2 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0019 | 0/0 | 6675 | 5 | 1 | 1 | 1 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0020 | 0/0 | 6675 | 5 | 0 | 1 | 3 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0021 | 1/0 | 6675 | 5 | 1 | 1 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0022 | 0/0 | 6675 | 5 | 1 | 1 | 3 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0023 | 0/0 | 6675 | 5 | 1 | 2 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0024 | 0/0 | 6675 | 4 | 4 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0025 | 0/0 | 6675 | 4 | 0 | 1 | 0 | 0 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0026 | 0/0 | 6675 | 4 | 0 | 0 | 1 | 0 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0027 | 0/0 | 6675 | 4 | 4 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0028 | 0/0 | 6675 | 4 | 0 | 1 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0029 | 0/0 | 6675 | 4 | 0 | 0 | 4 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0030 | 0/0 | 6675 | 3 | 2 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0031 | 0/0 | 6675 | 3 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0032 | 0/0 | 6675 | 3 | 0 | 1 | 1 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0033 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0034 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0035 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0036 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0037 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0038 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0039 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0040 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0041 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0042 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0043 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0044 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0045 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0046 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0047 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0048 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0049 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0050 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0051 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0052 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0053 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0054 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0055 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0056 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0057 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0058 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0059 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0060 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0061 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0062 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0063 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0064 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0065 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0066 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0067 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0068 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0069 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0070 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0071 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0072 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0073 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0074 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0075 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0076 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0077 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0078 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0079 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0080 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
c0081 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2458 | 89 | 20 | 25 | 32 | 5 | 7 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0002 | 0/0 | 2458 | 83 | 17 | 6 | 52 | 0 | 8 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0003 | 0/1 | 2458 | 53 | 16 | 14 | 8 | 5 | 9 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0004 | 0/0 | 2458 | 24 | 12 | 3 | 5 | 0 | 4 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0005 | 0/0 | 2458 | 24 | 2 | 8 | 10 | 3 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0006 | 1/0 | 2458 | 14 | 8 | 3 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0007 | 0/0 | 2458 | 3 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0008 | 0/0 | 2458 | 3 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0009 | 0/0 | 2458 | 2 | 0 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0010 | 0/0 | 2458 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0011 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0012 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0013 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0014 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0015 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0016 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0017 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0018 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
t0019 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
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 | 2 | 0 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
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 | 0/0 | 6675 | 25 | 0 | 0 | 25 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0002 | 0/0 | 6675 | 25 | 0 | 3 | 18 | 0 | 4 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0004 | 0/0 | 6675 | 12 | 0 | 1 | 10 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0074 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0003 | 0/0 | 6675 | 19 | 4 | 8 | 1 | 3 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0010 | 0/0 | 6675 | 9 | 1 | 5 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0019 | 0/0 | 6675 | 5 | 1 | 1 | 1 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0029 | 0/0 | 6675 | 4 | 0 | 0 | 4 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0070 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0079 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0005 | 0/0 | 6675 | 12 | 0 | 3 | 7 | 0 | 2 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0015 | 0/0 | 6675 | 6 | 0 | 2 | 3 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0018 | 0/1 | 6675 | 5 | 2 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0022 | 0/0 | 6675 | 5 | 1 | 1 | 3 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0026 | 0/0 | 6675 | 4 | 0 | 0 | 1 | 0 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0032 | 0/0 | 6675 | 3 | 0 | 1 | 1 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0073 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0078 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0007 | 0/0 | 6675 | 10 | 3 | 2 | 0 | 4 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0021 | 1/0 | 6675 | 5 | 1 | 1 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0023 | 0/0 | 6675 | 5 | 1 | 2 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0025 | 0/0 | 6675 | 4 | 0 | 1 | 0 | 0 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0040 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0050 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0059 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0067 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0069 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0006 | 0/0 | 6675 | 10 | 2 | 1 | 6 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0008 | 0/0 | 6675 | 10 | 0 | 6 | 3 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0011 | 0/0 | 6675 | 8 | 0 | 3 | 3 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0054 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0071 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0009 | 0/0 | 6675 | 9 | 0 | 6 | 3 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0020 | 0/0 | 6675 | 5 | 0 | 1 | 3 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0028 | 0/0 | 6675 | 4 | 0 | 1 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0076 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0013 | 0/0 | 6675 | 6 | 6 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0027 | 0/0 | 6675 | 4 | 4 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0041 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0056 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0063 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0008c0014 | 0/0 | 6675 | 6 | 0 | 0 | 6 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0008c0042 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0009c0016 | 0/0 | 6675 | 5 | 3 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0009c0030 | 0/0 | 6675 | 3 | 2 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0010c0012 | 0/0 | 6675 | 7 | 5 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0011c0017 | 0/0 | 6675 | 5 | 5 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0011c0036 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0012c0024 | 0/0 | 6675 | 4 | 4 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0013c0039 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0013c0062 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0014c0031 | 0/0 | 6675 | 3 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0015c0038 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0016c0035 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0017c0037 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0018c0033 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0019c0034 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0020c0075 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0021c0057 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0022c0058 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0023c0064 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0024c0066 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0025c0077 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0026c0051 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0027c0068 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0028c0065 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0029c0052 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0030c0055 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0031c0053 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0032c0060 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0033c0080 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0034c0072 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0035c0081 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0036c0061 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0037c0046 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0038c0047 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0039c0048 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0040c0049 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0041c0045 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0042c0043 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0043c0044 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 9132 | 25 | 0 | 0 | 25 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0002t0002 | 0/0 | 9132 | 25 | 0 | 3 | 18 | 0 | 4 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0004t0002 | 0/0 | 9132 | 10 | 0 | 1 | 8 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0004t0010 | 0/0 | 9132 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0001c0074t0002 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0003t0001 | 0/0 | 9132 | 18 | 3 | 8 | 1 | 3 | 3 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0003t0004 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0010t0001 | 0/0 | 9132 | 9 | 1 | 5 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0019t0001 | 0/0 | 9132 | 4 | 1 | 1 | 1 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0019t0018 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0029t0001 | 0/0 | 9132 | 4 | 0 | 0 | 4 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0070t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0002c0079t0001 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0005t0003 | 0/0 | 9132 | 11 | 0 | 3 | 7 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0005t0004 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0015t0004 | 0/0 | 9132 | 5 | 0 | 2 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0015t0014 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0018t0003 | 0/1 | 9132 | 5 | 2 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0022t0004 | 0/0 | 9132 | 4 | 1 | 1 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0022t0019 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0026t0003 | 0/0 | 9132 | 3 | 0 | 0 | 1 | 0 | 2 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0026t0004 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0032t0001 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0032t0004 | 0/0 | 9132 | 2 | 0 | 0 | 1 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0073t0004 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0003c0078t0003 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0007t0003 | 0/0 | 9132 | 10 | 3 | 2 | 0 | 4 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0021t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0021t0006 | 1/0 | 9132 | 4 | 0 | 1 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0023t0003 | 0/0 | 9132 | 5 | 1 | 2 | 0 | 1 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0025t0001 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0025t0003 | 0/0 | 9132 | 3 | 0 | 1 | 0 | 0 | 2 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0040t0002 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0040t0003 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0050t0003 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0059t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0067t0002 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0004c0069t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0006t0001 | 0/0 | 9132 | 10 | 2 | 1 | 6 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0008t0001 | 0/0 | 9132 | 10 | 0 | 6 | 3 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0011t0001 | 0/0 | 9132 | 6 | 0 | 2 | 3 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0011t0009 | 0/0 | 9132 | 2 | 0 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0054t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0005c0071t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0009t0005 | 0/0 | 9132 | 9 | 0 | 6 | 3 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0020t0005 | 0/0 | 9132 | 5 | 0 | 1 | 3 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0028t0005 | 0/0 | 9132 | 4 | 0 | 1 | 2 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0006c0076t0002 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0013t0002 | 0/0 | 9132 | 5 | 5 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0013t0006 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0027t0002 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0027t0006 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0027t0015 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0041t0006 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0041t0008 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0056t0008 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0007c0063t0006 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0008c0014t0001 | 0/0 | 9132 | 5 | 0 | 0 | 5 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0008c0014t0013 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0008c0042t0001 | 0/0 | 9132 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0009c0016t0003 | 0/0 | 9132 | 5 | 3 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0009c0030t0001 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0009c0030t0006 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0010c0012t0002 | 0/0 | 9132 | 7 | 5 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0011c0017t0004 | 0/0 | 9132 | 5 | 5 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0011c0036t0003 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0012c0024t0007 | 0/0 | 9132 | 3 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0012c0024t0012 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0013c0039t0001 | 0/0 | 9132 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0013c0062t0001 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0014c0031t0001 | 0/0 | 9132 | 3 | 3 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0015c0038t0005 | 0/0 | 9132 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0016c0035t0004 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0017c0037t0003 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0017c0037t0004 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0018c0033t0006 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0019c0034t0002 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0020c0075t0002 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0021c0057t0002 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0022c0058t0003 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0023c0064t0006 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0024c0066t0003 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0025c0077t0005 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0026c0051t0002 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0027c0068t0004 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0028c0065t0003 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0029c0052t0002 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0030c0055t0011 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0031c0053t0001 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0032c0060t0005 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0033c0080t0017 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0034c0072t0005 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0035c0081t0001 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0036c0061t0003 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0037c0046t0008 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0038c0047t0006 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0039c0048t0016 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0040c0049t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0041c0045t0005 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0042c0043t0003 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
a0043c0044t0001 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | copy fasta | chr1 | 169506951 | 169591481 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0004t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0001c0074t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0003t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0010t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0019t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0019t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0019t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0019t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0019t0018g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0029t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0029t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0029t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0029t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0070t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0002c0079t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0005t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0015t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0015t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0015t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0015t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0015t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0015t0014g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0018t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0018t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0018t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0018t0003g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0018t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0022t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0022t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0022t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0022t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0022t0019g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0026t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0026t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0026t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0026t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0032t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0032t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0032t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0073t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0003c0078t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0007t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0021t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0021t0006g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0021t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0021t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0021t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0023t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0023t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0023t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0023t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0023t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0025t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0025t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0025t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0025t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0040t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0040t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0050t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0059t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0067t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0004c0069t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0011t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0011t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0011t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0011t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0011t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0011t0009g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0054t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0005c0071t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0009t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0020t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0020t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0020t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0020t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0020t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0028t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0028t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0028t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0028t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0006c0076t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0013t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0013t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0013t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0013t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0013t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0013t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0027t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0027t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0027t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0027t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0041t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0041t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0056t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0007c0063t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0014t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0014t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0014t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0014t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0014t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0014t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0042t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0008c0042t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0016t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0016t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0016t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0016t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0016t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0030t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0030t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0009c0030t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0010c0012t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0011c0017t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0011c0017t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0011c0017t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0011c0017t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0011c0036t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0011c0036t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0012c0024t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0012c0024t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0012c0024t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0012c0024t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0013c0039t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0013c0039t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0013c0062t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0014c0031t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0014c0031t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0014c0031t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0015c0038t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0015c0038t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0016c0035t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0016c0035t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0017c0037t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0017c0037t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0018c0033t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0018c0033t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0019c0034t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0019c0034t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0020c0075t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0021c0057t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0022c0058t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0023c0064t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0024c0066t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0025c0077t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0026c0051t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0027c0068t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0028c0065t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0029c0052t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0030c0055t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0031c0053t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0032c0060t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0033c0080t0017g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0034c0072t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0035c0081t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0036c0061t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0037c0046t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0038c0047t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0039c0048t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0040c0049t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0041c0045t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0042c0043t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
a0043c0044t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0019 | t0001 | g0053 | EUR | GBR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00099 | hp2 | a0004 | c0007 | t0003 | g0267 | EUR | GBR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00140 | hp1 | a0004 | c0021 | t0006 | g0245 | EUR | GBR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0248 | EUR | GBR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00280 | hp1 | a0004 | c0007 | t0003 | g0234 | EUR | FIN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00280 | hp2 | a0025 | c0077 | t0005 | g0213 | EUR | FIN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00408 | hp1 | a0005 | c0008 | t0001 | g0192 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00408 | hp2 | a0008 | c0014 | t0013 | g0132 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00423 | hp1 | a0003 | c0005 | t0003 | g0032 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00423 | hp2 | a0008 | c0014 | t0001 | g0018 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00438 | hp2 | a0003 | c0015 | t0004 | g0088 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00639 | hp1 | a0004 | c0025 | t0003 | g0126 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00639 | hp2 | a0005 | c0008 | t0001 | g0171 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00673 | hp2 | a0031 | c0053 | t0001 | g0099 | EAS | CHS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00733 | hp1 | a0003 | c0005 | t0003 | g0214 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00733 | hp2 | a0003 | c0022 | t0004 | g0256 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00735 | hp1 | a0005 | c0008 | t0001 | g0165 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00735 | hp2 | a0004 | c0021 | t0006 | g0295 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00738 | hp1 | a0005 | c0011 | t0009 | g0001 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG00738 | hp2 | a0003 | c0018 | t0003 | g0026 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01069 | hp1 | a0004 | c0023 | t0003 | g0155 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01069 | hp2 | a0006 | c0009 | t0005 | g0078 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01071 | hp1 | a0004 | c0023 | t0003 | g0186 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01071 | hp2 | a0006 | c0009 | t0005 | g0079 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01074 | hp1 | a0006 | c0020 | t0005 | g0263 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0257 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01081 | hp2 | a0024 | c0066 | t0003 | g0270 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01099 | hp1 | a0004 | c0007 | t0003 | g0266 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0258 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01109 | hp1 | a0009 | c0016 | t0003 | g0065 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01109 | hp2 | a0010 | c0012 | t0002 | g0062 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01168 | hp1 | a0002 | c0003 | t0001 | g0025 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01168 | hp2 | a0005 | c0011 | t0001 | g0296 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01169 | hp1 | a0005 | c0011 | t0001 | g0269 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01175 | hp1 | a0004 | c0007 | t0003 | g0259 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0268 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0224 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01243 | hp2 | a0010 | c0012 | t0002 | g0063 | AMR | PUR | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01255 | hp1 | a0002 | c0079 | t0001 | g0216 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01255 | hp2 | a0006 | c0009 | t0005 | g0081 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01256 | hp1 | a0006 | c0028 | t0005 | g0219 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01256 | hp2 | a0002 | c0010 | t0001 | g0183 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01258 | hp1 | a0006 | c0009 | t0005 | g0138 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01258 | hp2 | a0002 | c0010 | t0001 | g0181 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01261 | hp1 | a0002 | c0019 | t0001 | g0104 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01261 | hp2 | a0003 | c0005 | t0003 | g0218 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01346 | hp1 | a0002 | c0010 | t0001 | g0177 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01346 | hp2 | a0009 | c0030 | t0006 | g0074 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01361 | hp1 | a0009 | c0016 | t0003 | g0051 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01361 | hp2 | a0005 | c0006 | t0001 | g0122 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01433 | hp1 | a0002 | c0010 | t0001 | g0185 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01433 | hp2 | a0006 | c0009 | t0005 | g0055 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01496 | hp1 | a0002 | c0010 | t0001 | g0210 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01515 | hp1 | a0006 | c0020 | t0005 | g0225 | EUR | IBS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01515 | hp2 | a0002 | c0003 | t0001 | g0005 | EUR | IBS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01517 | hp1 | a0004 | c0007 | t0003 | g0264 | EUR | IBS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0005 | EUR | IBS | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01884 | hp1 | a0005 | c0006 | t0001 | g0280 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01884 | hp2 | a0012 | c0024 | t0007 | g0072 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01934 | hp1 | a0005 | c0008 | t0001 | g0170 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01952 | hp1 | a0003 | c0032 | t0001 | g0179 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01952 | hp2 | a0006 | c0009 | t0005 | g0082 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01981 | hp1 | a0023 | c0064 | t0006 | g0250 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01981 | hp2 | a0005 | c0008 | t0001 | g0203 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01993 | hp1 | a0003 | c0005 | t0003 | g0217 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01993 | hp2 | a0005 | c0008 | t0001 | g0168 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02004 | hp1 | a0028 | c0065 | t0003 | g0260 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02004 | hp2 | a0005 | c0008 | t0001 | g0190 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02040 | hp2 | a0005 | c0011 | t0001 | g0255 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02055 | hp1 | a0007 | c0063 | t0006 | g0261 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02055 | hp2 | a0007 | c0013 | t0002 | g0077 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02056 | hp1 | a0003 | c0015 | t0004 | g0089 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02071 | hp1 | a0035 | c0081 | t0001 | g0167 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02132 | hp2 | a0005 | c0011 | t0001 | g0004 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02135 | hp2 | a0005 | c0006 | t0001 | g0080 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02145 | hp1 | a0007 | c0013 | t0002 | g0041 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02145 | hp2 | a0016 | c0035 | t0004 | g0069 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CDX | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02155 | hp2 | a0001 | c0004 | t0002 | g0024 | EAS | CDX | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02258 | hp1 | a0005 | c0071 | t0001 | g0293 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02258 | hp2 | a0017 | c0037 | t0003 | g0045 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02273 | hp1 | a0001 | c0004 | t0002 | g0232 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02273 | hp2 | a0003 | c0015 | t0004 | g0123 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02280 | hp1 | a0037 | c0046 | t0008 | g0291 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02280 | hp2 | a0019 | c0034 | t0002 | g0006 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02293 | hp2 | a0036 | c0061 | t0003 | g0083 | AMR | PEL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02523 | hp2 | a0005 | c0011 | t0001 | g0004 | EAS | KHV | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02572 | hp1 | a0004 | c0023 | t0003 | g0148 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02572 | hp2 | a0010 | c0012 | t0002 | g0042 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02602 | hp1 | a0004 | c0025 | t0003 | g0084 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02602 | hp2 | a0005 | c0006 | t0001 | g0294 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02615 | hp1 | a0007 | c0027 | t0006 | g0271 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02615 | hp2 | a0021 | c0057 | t0002 | g0298 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02622 | hp1 | a0004 | c0059 | t0001 | g0300 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02622 | hp2 | a0002 | c0003 | t0004 | g0275 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02630 | hp1 | a0003 | c0073 | t0004 | g0039 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02630 | hp2 | a0009 | c0016 | t0003 | g0056 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02647 | hp1 | a0017 | c0037 | t0004 | g0046 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02647 | hp2 | a0007 | c0013 | t0002 | g0285 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02723 | hp1 | a0002 | c0070 | t0001 | g0277 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02723 | hp2 | a0010 | c0012 | t0002 | g0050 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02735 | hp1 | a0003 | c0015 | t0004 | g0040 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02735 | hp2 | a0004 | c0007 | t0003 | g0251 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02738 | hp1 | a0004 | c0023 | t0003 | g0152 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02809 | hp1 | a0010 | c0012 | t0002 | g0064 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02809 | hp2 | a0011 | c0017 | t0004 | g0002 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0220 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02818 | hp2 | a0029 | c0052 | t0002 | g0281 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02886 | hp1 | a0012 | c0024 | t0012 | g0044 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02886 | hp2 | a0004 | c0007 | t0003 | g0012 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02895 | hp1 | a0011 | c0017 | t0004 | g0066 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02895 | hp2 | a0018 | c0033 | t0006 | g0008 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02896 | hp1 | a0004 | c0007 | t0003 | g0022 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02896 | hp2 | a0004 | c0069 | t0001 | g0288 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02897 | hp1 | a0011 | c0017 | t0004 | g0068 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02897 | hp2 | a0004 | c0007 | t0003 | g0021 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02922 | hp1 | a0010 | c0012 | t0002 | g0061 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02922 | hp2 | a0007 | c0041 | t0008 | g0017 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02965 | hp1 | a0014 | c0031 | t0001 | g0058 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02965 | hp2 | a0009 | c0030 | t0001 | g0038 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03041 | hp1 | a0012 | c0024 | t0007 | g0047 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03041 | hp2 | a0011 | c0036 | t0003 | g0286 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03098 | hp1 | a0007 | c0027 | t0002 | g0273 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03098 | hp2 | a0007 | c0056 | t0008 | g0290 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03130 | hp1 | a0033 | c0080 | t0017 | g0215 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03130 | hp2 | a0003 | c0022 | t0004 | g0016 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03139 | hp1 | a0040 | c0049 | t0001 | g0036 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03139 | hp2 | a0016 | c0035 | t0004 | g0070 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03195 | hp1 | a0004 | c0067 | t0002 | g0276 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03195 | hp2 | a0012 | c0024 | t0007 | g0067 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03225 | hp1 | a0038 | c0047 | t0006 | g0057 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03225 | hp2 | a0007 | c0027 | t0006 | g0272 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03453 | hp1 | a0030 | c0055 | t0011 | g0076 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03453 | hp2 | a0022 | c0058 | t0003 | g0299 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03486 | hp1 | a0007 | c0041 | t0006 | g0014 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03486 | hp2 | a0014 | c0031 | t0001 | g0052 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0254 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03491 | hp2 | a0003 | c0078 | t0003 | g0202 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0253 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03492 | hp2 | a0020 | c0075 | t0002 | g0184 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03516 | hp1 | a0005 | c0054 | t0001 | g0054 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03516 | hp2 | a0007 | c0013 | t0002 | g0282 | AFR | ESN | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03540 | hp1 | a0004 | c0040 | t0003 | g0289 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03540 | hp2 | a0007 | c0013 | t0002 | g0278 | AFR | GWD | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03579 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03579 | hp2 | a0011 | c0017 | t0004 | g0060 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03654 | hp2 | a0005 | c0011 | t0009 | g0001 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03669 | hp1 | a0003 | c0018 | t0003 | g0117 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03669 | hp2 | a0003 | c0032 | t0004 | g0187 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03688 | hp1 | a0002 | c0019 | t0018 | g0121 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03688 | hp2 | a0004 | c0025 | t0001 | g0108 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03704 | hp1 | a0001 | c0004 | t0002 | g0249 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03704 | hp2 | a0005 | c0008 | t0001 | g0159 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03710 | hp2 | a0002 | c0003 | t0001 | g0019 | SAS | PJL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03831 | hp1 | a0003 | c0026 | t0003 | g0236 | SAS | BEB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03831 | hp2 | a0003 | c0026 | t0004 | g0222 | SAS | BEB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03942 | hp1 | a0002 | c0010 | t0001 | g0201 | SAS | BEB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03942 | hp2 | a0003 | c0005 | t0004 | g0151 | SAS | BEB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04115 | hp1 | a0003 | c0005 | t0003 | g0156 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04115 | hp2 | a0004 | c0025 | t0003 | g0115 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04184 | hp1 | a0006 | c0028 | t0005 | g0147 | SAS | BEB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04184 | hp2 | a0026 | c0051 | t0002 | g0109 | SAS | BEB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04204 | hp1 | a0004 | c0021 | t0006 | g0265 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04204 | hp2 | a0003 | c0026 | t0003 | g0252 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04228 | hp1 | a0006 | c0076 | t0002 | g0208 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0211 | SAS | STU | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18522 | hp1 | a0032 | c0060 | t0005 | g0297 | AFR | YRI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18522 | hp2 | a0007 | c0013 | t0006 | g0283 | AFR | YRI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18612 | hp2 | a0003 | c0005 | t0003 | g0027 | EAS | CHB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | CHB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18747 | hp2 | a0005 | c0006 | t0001 | g0131 | EAS | CHB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18906 | hp1 | a0007 | c0027 | t0015 | g0274 | AFR | YRI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18906 | hp2 | a0004 | c0050 | t0003 | g0279 | AFR | YRI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18939 | hp1 | a0003 | c0015 | t0014 | g0085 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18939 | hp2 | a0003 | c0026 | t0003 | g0233 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18941 | hp1 | a0002 | c0029 | t0001 | g0180 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18947 | hp1 | a0005 | c0008 | t0001 | g0209 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18947 | hp2 | a0003 | c0005 | t0003 | g0033 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18948 | hp1 | a0005 | c0008 | t0001 | g0166 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18948 | hp2 | a0001 | c0004 | t0010 | g0247 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18951 | hp1 | a0001 | c0004 | t0002 | g0227 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18951 | hp2 | a0008 | c0042 | t0001 | g0164 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18952 | hp1 | a0006 | c0009 | t0005 | g0106 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18956 | hp1 | a0005 | c0006 | t0001 | g0118 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18956 | hp2 | a0001 | c0004 | t0002 | g0239 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18957 | hp1 | a0001 | c0074 | t0002 | g0120 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18957 | hp2 | a0001 | c0004 | t0002 | g0023 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18960 | hp1 | a0015 | c0038 | t0005 | g0142 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18963 | hp1 | a0005 | c0006 | t0001 | g0093 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18971 | hp1 | a0006 | c0009 | t0005 | g0107 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18971 | hp2 | a0008 | c0014 | t0001 | g0144 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18973 | hp1 | a0002 | c0010 | t0001 | g0149 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18973 | hp2 | a0003 | c0022 | t0019 | g0235 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18975 | hp1 | a0003 | c0005 | t0003 | g0029 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18979 | hp1 | a0006 | c0028 | t0005 | g0195 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18985 | hp1 | a0001 | c0004 | t0002 | g0226 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18985 | hp2 | a0008 | c0014 | t0001 | g0116 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18987 | hp2 | a0001 | c0004 | t0010 | g0231 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18988 | hp1 | a0006 | c0020 | t0005 | g0243 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18991 | hp1 | a0006 | c0009 | t0005 | g0097 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18991 | hp2 | a0002 | c0029 | t0001 | g0175 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18992 | hp2 | a0003 | c0022 | t0004 | g0229 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18993 | hp1 | a0013 | c0039 | t0001 | g0139 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18995 | hp1 | a0002 | c0019 | t0001 | g0143 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18998 | hp1 | a0008 | c0014 | t0001 | g0096 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA18999 | hp2 | a0015 | c0038 | t0005 | g0112 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19001 | hp1 | a0003 | c0005 | t0003 | g0153 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19009 | hp1 | a0001 | c0004 | t0002 | g0230 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19010 | hp1 | a0003 | c0032 | t0004 | g0191 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19011 | hp2 | a0013 | c0062 | t0001 | g0242 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19012 | hp1 | a0002 | c0029 | t0001 | g0182 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19030 | hp1 | a0010 | c0012 | t0002 | g0037 | AFR | LWK | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19030 | hp2 | a0039 | c0048 | t0016 | g0073 | AFR | LWK | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19043 | hp1 | a0014 | c0031 | t0001 | g0035 | AFR | LWK | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0013 | AFR | LWK | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19058 | hp1 | a0006 | c0028 | t0005 | g0154 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19063 | hp2 | a0003 | c0005 | t0003 | g0034 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19064 | hp1 | a0005 | c0006 | t0001 | g0119 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19066 | hp1 | a0003 | c0005 | t0003 | g0031 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19067 | hp1 | a0005 | c0006 | t0001 | g0130 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19070 | hp2 | a0008 | c0014 | t0001 | g0095 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19074 | hp1 | a0002 | c0010 | t0001 | g0150 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19076 | hp1 | a0002 | c0029 | t0001 | g0172 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19076 | hp2 | a0001 | c0004 | t0002 | g0240 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19078 | hp2 | a0006 | c0020 | t0005 | g0237 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19082 | hp1 | a0008 | c0042 | t0001 | g0204 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19085 | hp1 | a0006 | c0020 | t0005 | g0223 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19085 | hp2 | a0003 | c0022 | t0004 | g0241 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19089 | hp1 | a0001 | c0004 | t0002 | g0228 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19089 | hp2 | a0013 | c0039 | t0001 | g0127 | EAS | JPT | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19240 | hp1 | a0011 | c0036 | t0003 | g0049 | AFR | YRI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA19240 | hp2 | a0019 | c0034 | t0002 | g0009 | AFR | YRI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20129 | hp1 | a0002 | c0010 | t0001 | g0206 | AFR | ASW | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20129 | hp2 | a0003 | c0018 | t0003 | g0048 | AFR | ASW | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20752 | hp1 | a0041 | c0045 | t0005 | g0075 | EUR | TSI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20752 | hp2 | a0004 | c0007 | t0003 | g0246 | EUR | TSI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20805 | hp1 | a0004 | c0023 | t0003 | g0198 | EUR | TSI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20805 | hp2 | a0005 | c0011 | t0001 | g0020 | EUR | TSI | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01123 | hp1 | a0003 | c0015 | t0004 | g0124 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0262 | AMR | CLM | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02109 | hp1 | a0027 | c0068 | t0004 | g0287 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02109 | hp2 | a0018 | c0033 | t0006 | g0011 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02486 | hp1 | a0009 | c0030 | t0001 | g0059 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02486 | hp2 | a0004 | c0040 | t0002 | g0301 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02559 | hp1 | a0002 | c0019 | t0001 | g0284 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG02559 | hp2 | a0011 | c0017 | t0004 | g0002 | AFR | ACB | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03471 | hp1 | a0042 | c0043 | t0003 | g0010 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG03471 | hp2 | a0043 | c0044 | t0001 | g0007 | AFR | MSL | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG06807 | hp1 | a0034 | c0072 | t0005 | g0292 | AFR | USA | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
HG06807 | hp2 | a0009 | c0016 | t0003 | g0071 | AFR | USA | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20300 | hp1 | a0004 | c0021 | t0001 | g0221 | AFR | USA | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA20300 | hp2 | a0005 | c0006 | t0001 | g0125 | AFR | USA | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA21309 | hp1 | a0009 | c0016 | t0003 | g0043 | AFR | LWK | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
NA21309 | hp2 | a0003 | c0018 | t0003 | g0091 | AFR | LWK | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
homoSapiens_chm13v2 | hp1 | a0003 | c0018 | t0003 | g0114 | REF | REF | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
homoSapiens_grch38 | hp1 | a0004 | c0021 | t0006 | g0244 | REF | REF | F5_chr1_169506951_169591481 | F5 | chr1 | 169506951 | 169591481 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169514323
|
T | C | 4 | a0006a0015a0025others(1): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
missense_variant | MODERATE | c.6665A>G | p.Asp2222Gly | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 6760/9132 | 6665/6675 | 2222/2224 | chr1 | 169514323 | ||
chr1:169514434
|
T | C | 1 | a0033 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.6554A>G | p.Lys2185Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 6649/9132 | 6554/6675 | 2185/2224 | chr1 | 169514434 | ||
chr1:169520626
|
C | A | 1 | a0020 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.6087G>T | p.Glu2029Asp | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/25 | 6182/9132 | 6087/6675 | 2029/2224 | chr1 | 169520626 | ||
chr1:169523215
|
G | C | 1 | a0028 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.6030C>G | p.Asn2010Lys | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/25 | 6125/9132 | 6030/6675 | 2010/2224 | chr1 | 169523215 | ||
chr1:169528054
|
C | T | 2 | a0017a0027 | 3 | HG02109.hp1 HG02258.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.5460G>A | p.Met1820Ile | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/25 | 5555/9132 | 5460/6675 | 1820/2224 | chr1 | 169528054 | ||
chr1:169528076
|
T | C | 1 | a0040 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.5438A>G | p.Tyr1813Cys | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/25 | 5533/9132 | 5438/6675 | 1813/2224 | chr1 | 169528076 | ||
chr1:169529737
|
T | C | 13 | a0002a0005a0006others(10): Show | 110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
missense_variant | MODERATE | c.5290A>G | p.Met1764Val | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/25 | 5385/9132 | 5290/6675 | 1764/2224 | chr1 | 169529737 | ||
chr1:169540880
|
G | A | 3 | a0005a0008a0031 | 39 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(36): Show |
missense_variant | MODERATE | c.4210C>T | p.Pro1404Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 4305/9132 | 4210/6675 | 1404/2224 | chr1 | 169540880 | ||
chr1:169540901
|
G | A | 3 | a0001a0020a0026 | 65 | HG00438.hp1 HG00673.hp1 HG01496.hp2 others(62): Show |
missense_variant | MODERATE | c.4189C>T | p.Leu1397Phe | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 4284/9132 | 4189/6675 | 1397/2224 | chr1 | 169540901 | ||
chr1:169541110
|
T | C | 4 | a0006a0015a0036others(1): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
missense_variant | MODERATE | c.3980A>G | p.His1327Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 4075/9132 | 3980/6675 | 1327/2224 | chr1 | 169541110 | ||
chr1:169541237
|
G | T | 4 | a0003a0011a0016others(1): Show | 47 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
missense_variant | MODERATE | c.3853C>A | p.Leu1285Ile | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3948/9132 | 3853/6675 | 1285/2224 | chr1 | 169541237 | ||
chr1:169541245
|
T | C | 2 | a0033a0034 | 2 | HG03130.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.3845A>G | p.His1282Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3940/9132 | 3845/6675 | 1282/2224 | chr1 | 169541245 | ||
chr1:169541536
|
A | T | 1 | a0031 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.3554T>A | p.Val1185Asp | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3649/9132 | 3554/6675 | 1185/2224 | chr1 | 169541536 | ||
chr1:169541652
|
G | C | 4 | a0010a0019a0021others(1): Show | 11 | HG01109.hp2 HG01243.hp2 HG02280.hp2 others(8): Show |
missense_variant | MODERATE | c.3438C>G | p.His1146Gln | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3533/9132 | 3438/6675 | 1146/2224 | chr1 | 169541652 | ||
chr1:169541833
|
A | G | 1 | a0032 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3257T>C | p.Leu1086Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3352/9132 | 3257/6675 | 1086/2224 | chr1 | 169541833 | ||
chr1:169541928
|
T | G | 1 | a0033 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3162A>C | p.Glu1054Asp | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3257/9132 | 3162/6675 | 1054/2224 | chr1 | 169541928 | ||
chr1:169542151
|
C | A | 1 | a0030 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.2939G>T | p.Arg980Leu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3034/9132 | 2939/6675 | 980/2224 | chr1 | 169542151 | ||
chr1:169542184
|
T | C | 1 | a0038 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2906A>G | p.Asn969Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3001/9132 | 2906/6675 | 969/2224 | chr1 | 169542184 | ||
chr1:169542317
|
T | C | 11 | a0002a0005a0008others(8): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
missense_variant | MODERATE | c.2773A>G | p.Lys925Glu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2868/9132 | 2773/6675 | 925/2224 | chr1 | 169542317 | ||
chr1:169542496
|
T | C | 11 | a0002a0005a0008others(8): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
missense_variant | MODERATE | c.2594A>G | p.His865Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2689/9132 | 2594/6675 | 865/2224 | chr1 | 169542496 | ||
chr1:169542517
|
T | C | 11 | a0002a0005a0008others(8): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
missense_variant | MODERATE | c.2573A>G | p.Lys858Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2668/9132 | 2573/6675 | 858/2224 | chr1 | 169542517 | ||
chr1:169542640
|
T | G | 4 | a0006a0015a0036others(1): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
missense_variant | MODERATE | c.2450A>C | p.Asn817Thr | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2545/9132 | 2450/6675 | 817/2224 | chr1 | 169542640 | ||
chr1:169542665
|
G | A | 3 | a0012a0022a0042 | 6 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(3): Show |
missense_variant | MODERATE | c.2425C>T | p.Pro809Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2520/9132 | 2425/6675 | 809/2224 | chr1 | 169542665 | ||
chr1:169542961
|
T | C | 2 | a0033a0034 | 2 | HG03130.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.2129A>G | p.His710Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2224/9132 | 2129/6675 | 710/2224 | chr1 | 169542961 | ||
chr1:169542985
|
G | A | 1 | a0024 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.2105C>T | p.Thr702Ile | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2200/9132 | 2105/6675 | 702/2224 | chr1 | 169542985 | ||
chr1:169543068
|
C | A | 1 | a0035 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2022G>T | p.Lys674Asn | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2117/9132 | 2022/6675 | 674/2224 | chr1 | 169543068 | ||
chr1:169549811
|
C | T | 1 | a0023 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1601G>A | p.Arg534Gln | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/25 | 1696/9132 | 1601/6675 | 534/2224 | chr1 | 169549811 | ||
chr1:169549874
|
C | T | 15 | a0001a0007a0008others(12): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
missense_variant | MODERATE | c.1538G>A | p.Arg513Lys | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/25 | 1633/9132 | 1538/6675 | 513/2224 | chr1 | 169549874 | ||
chr1:169552615
|
A | G | 3 | a0006a0036a0041 | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
missense_variant | MODERATE | c.1238T>C | p.Met413Thr | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/25 | 1333/9132 | 1238/6675 | 413/2224 | chr1 | 169552615 | ||
chr1:169572275
|
C | G | 12 | a0009a0010a0011others(9): Show | 38 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(35): Show |
missense_variant | MODERATE | c.319G>C | p.Asp107His | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/25 | 414/9132 | 319/6675 | 107/2224 | chr1 | 169572275 | ||
chr1:169586344
|
C | T | 4 | a0018a0019a0042others(1): Show | 6 | HG02109.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.43G>A | p.Gly15Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/25 | 138/9132 | 43/6675 | 15/2224 | chr1 | 169586344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169514337
|
T | C | 1 | a0003c0078 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.6651A>G | p.Glu2217Glu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 6746/9132 | 6651/6675 | 2217/2224 | chr1 | 169514337 | ||
chr1:169523296
|
G | A | 1 | a0034c0072 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.5949C>T | p.His1983His | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/25 | 6044/9132 | 5949/6675 | 1983/2224 | chr1 | 169523296 | ||
chr1:169530972
|
T | C | 8 | a0005c0006a0005c0008a0005c0011others(5): Show | 39 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(36): Show |
synonymous_variant | LOW | c.5022A>G | p.Gly1674Gly | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/25 | 5117/9132 | 5022/6675 | 1674/2224 | chr1 | 169530972 | ||
chr1:169536554
|
G | A | 1 | a0033c0080 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.4923C>T | p.Leu1641Leu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/25 | 5018/9132 | 4923/6675 | 1641/2224 | chr1 | 169536554 | ||
chr1:169540527
|
A | G | 2 | a0005c0054a0005c0071 | 2 | HG02258.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.4563T>C | p.Asp1521Asp | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 4658/9132 | 4563/6675 | 1521/2224 | chr1 | 169540527 | ||
chr1:169540995
|
G | A | 8 | a0004c0007a0004c0023a0004c0025others(5): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
synonymous_variant | LOW | c.4095C>T | p.Thr1365Thr | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 4190/9132 | 4095/6675 | 1365/2224 | chr1 | 169540995 | ||
chr1:169541142
|
G | A | 22 | a0002c0003a0002c0010a0002c0019others(19): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
synonymous_variant | LOW | c.3948C>T | p.Leu1316Leu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 4043/9132 | 3948/6675 | 1316/2224 | chr1 | 169541142 | ||
chr1:169541286
|
A | G | 29 | a0002c0003a0002c0010a0002c0019others(26): Show | 112 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
synonymous_variant | LOW | c.3804T>C | p.Ser1268Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3899/9132 | 3804/6675 | 1268/2224 | chr1 | 169541286 | ||
chr1:169541586
|
T | G | 2 | a0002c0029a0035c0081 | 5 | HG02071.hp1 NA18941.hp1 NA18991.hp2 others(2): Show |
synonymous_variant | LOW | c.3504A>C | p.Thr1168Thr | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3599/9132 | 3504/6675 | 1168/2224 | chr1 | 169541586 | ||
chr1:169542165
|
G | A | 1 | a0002c0079 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.2925C>T | p.Pro975Pro | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 3020/9132 | 2925/6675 | 975/2224 | chr1 | 169542165 | ||
chr1:169542789
|
T | C | 22 | a0002c0003a0002c0010a0002c0019others(19): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
synonymous_variant | LOW | c.2301A>G | p.Ser767Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2396/9132 | 2301/6675 | 767/2224 | chr1 | 169542789 | ||
chr1:169542801
|
T | C | 7 | a0006c0009a0006c0020a0006c0028others(4): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
synonymous_variant | LOW | c.2289A>G | p.Glu763Glu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2384/9132 | 2289/6675 | 763/2224 | chr1 | 169542801 | ||
chr1:169542855
|
A | G | 22 | a0002c0003a0002c0010a0002c0019others(19): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
synonymous_variant | LOW | c.2235T>C | p.Asn745Asn | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2330/9132 | 2235/6675 | 745/2224 | chr1 | 169542855 | ||
chr1:169542882
|
G | A | 22 | a0002c0003a0002c0010a0002c0019others(19): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
synonymous_variant | LOW | c.2208C>T | p.Ile736Ile | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/25 | 2303/9132 | 2208/6675 | 736/2224 | chr1 | 169542882 | ||
chr1:169544345
|
G | T | 5 | a0006c0009a0006c0020a0006c0028others(2): Show | 20 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(17): Show |
synonymous_variant | LOW | c.1926C>A | p.Thr642Thr | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/25 | 2021/9132 | 1926/6675 | 642/2224 | chr1 | 169544345 | ||
chr1:169544486
|
C | T | 1 | a0039c0048 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1785G>A | p.Glu595Glu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/25 | 1880/9132 | 1785/6675 | 595/2224 | chr1 | 169544486 | ||
chr1:169546488
|
C | T | 6 | a0006c0009a0006c0020a0006c0028others(3): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1716G>A | p.Glu572Glu | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/25 | 1811/9132 | 1716/6675 | 572/2224 | chr1 | 169546488 | ||
chr1:169549873
|
T | C | 1 | a0007c0063 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1539A>G | p.Arg513Arg | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/25 | 1634/9132 | 1539/6675 | 513/2224 | chr1 | 169549873 | ||
chr1:169550656
|
G | A | 6 | a0006c0009a0006c0020a0006c0028others(3): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1380C>T | p.Asn460Asn | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/25 | 1475/9132 | 1380/6675 | 460/2224 | chr1 | 169550656 | ||
chr1:169552611
|
T | C | 5 | a0003c0015a0003c0022a0003c0032others(2): Show | 20 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(17): Show |
synonymous_variant | LOW | c.1242A>G | p.Lys414Lys | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/25 | 1337/9132 | 1242/6675 | 414/2224 | chr1 | 169552611 | ||
chr1:169556782
|
G | A | 2 | a0004c0067a0007c0027 | 5 | HG02615.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
synonymous_variant | LOW | c.816C>T | p.Asn272Asn | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/25 | 911/9132 | 816/6675 | 272/2224 | chr1 | 169556782 | ||
chr1:169559265
|
C | T | 1 | a0020c0075 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.618G>A | p.Thr206Thr | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/25 | 713/9132 | 618/6675 | 206/2224 | chr1 | 169559265 | ||
chr1:169560576
|
C | G | 10 | a0004c0040a0004c0059a0007c0056others(7): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
synonymous_variant | LOW | c.564G>C | p.Gly188Gly | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/25 | 659/9132 | 564/6675 | 188/2224 | chr1 | 169560576 | ||
chr1:169560588
|
C | A | 38 | a0001c0001a0001c0074a0002c0019others(35): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
synonymous_variant | LOW | c.552G>T | p.Ser184Ser | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/25 | 647/9132 | 552/6675 | 184/2224 | chr1 | 169560588 | ||
chr1:169560735
|
C | T | 32 | a0001c0001a0001c0074a0002c0019others(29): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
synonymous_variant | LOW | c.405G>A | p.Ala135Ala | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/25 | 500/9132 | 405/6675 | 135/2224 | chr1 | 169560735 | ||
chr1:169572306
|
G | A | 1 | a0001c0074 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.288C>T | p.Asp96Asp | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/25 | 383/9132 | 288/6675 | 96/2224 | chr1 | 169572306 | ||
chr1:169582444
|
T | C | 16 | a0001c0002a0002c0010a0002c0029others(13): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
synonymous_variant | LOW | c.237A>G | p.Gln79Gln | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/25 | 332/9132 | 237/6675 | 79/2224 | chr1 | 169582444 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169511985
|
C | G | 90 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(87): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*2328G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 2328 | chr1 | 169511985 | |||||
chr1:169512290
|
A | C | 1 | a0008c0014t0013 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2023T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 2023 | chr1 | 169512290 | |||||
chr1:169512388
|
C | G | 1 | a0033c0080t0017 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1925G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1925 | chr1 | 169512388 | |||||
chr1:169512493
|
T | G | 8 | a0006c0009t0005a0006c0020t0005a0006c0028t0005others(5): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1820A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1820 | chr1 | 169512493 | |||||
chr1:169512712
|
G | A | 29 | a0002c0003t0001a0002c0010t0001a0002c0019t0001others(26): Show | 93 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1601C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1601 | chr1 | 169512712 | |||||
chr1:169512788
|
G | A | 1 | a0012c0024t0012 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1525 | chr1 | 169512788 | |||||
chr1:169512825
|
A | G | 3 | a0007c0041t0008a0007c0056t0008a0037c0046t0008 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1488T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1488 | chr1 | 169512825 | |||||
chr1:169512877
|
A | T | 17 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(14): Show | 86 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1436T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1436 | chr1 | 169512877 | |||||
chr1:169512989
|
A | G | 1 | a0007c0027t0015 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1324 | chr1 | 169512989 | |||||
chr1:169513056
|
T | G | 1 | a0003c0015t0014 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1257 | chr1 | 169513056 | |||||
chr1:169513067
|
G | A | 8 | a0006c0009t0005a0006c0020t0005a0006c0028t0005others(5): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1246C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1246 | chr1 | 169513067 | |||||
chr1:169513195
|
C | T | 2 | a0012c0024t0007a0012c0024t0012 | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1118G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1118 | chr1 | 169513195 | |||||
chr1:169513198
|
G | A | 34 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(31): Show | 139 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1115C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1115 | chr1 | 169513198 | |||||
chr1:169513242
|
C | A | 1 | a0039c0048t0016 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 1071 | chr1 | 169513242 | |||||
chr1:169513440
|
G | A | 8 | a0006c0009t0005a0006c0020t0005a0006c0028t0005others(5): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*873C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 873 | chr1 | 169513440 | |||||
chr1:169513512
|
C | G | 1 | a0001c0004t0010 | 2 | NA18948.hp2 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*801G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 801 | chr1 | 169513512 | |||||
chr1:169513513
|
T | C | 1 | a0001c0004t0010 | 2 | NA18948.hp2 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*800A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 800 | chr1 | 169513513 | |||||
chr1:169513514
|
C | A | 1 | a0001c0004t0010 | 2 | NA18948.hp2 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*799G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 799 | chr1 | 169513514 | |||||
chr1:169513518
|
G | C | 1 | a0001c0004t0010 | 2 | NA18948.hp2 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*795C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 795 | chr1 | 169513518 | |||||
chr1:169513832
|
A | G | 1 | a0030c0055t0011 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 481 | chr1 | 169513832 | |||||
chr1:169513837
|
G | A | 2 | a0002c0019t0018a0033c0080t0017 | 2 | HG03130.hp1 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*476C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 476 | chr1 | 169513837 | |||||
chr1:169513937
|
T | A | 3 | a0007c0041t0008a0007c0056t0008a0037c0046t0008 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 376 | chr1 | 169513937 | |||||
chr1:169514164
|
G | C | 1 | a0003c0022t0019 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 25/25 | 149 | chr1 | 169514164 | |||||
chr1:169586426
|
A | G | 1 | a0005c0011t0009 | 2 | HG00738.hp1 HG03654.hp2 |
5_prime_UTR_variant | MODIFIER | c.-40T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/25 | 40 | chr1 | 169586426 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:169514524
|
T | G | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6529-65A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169514524 | ||||||
chr1:169514606
|
C | T | 89 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(86): Show | 93 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.6529-147G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169514606 | ||||||
chr1:169514738
|
C | T | 1 | a0003c0005t0003g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.6529-279G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169514738 | ||||||
chr1:169514884
|
T | C | 1 | a0024c0066t0003g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6529-425A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169514884 | ||||||
chr1:169514937
|
T | C | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6529-478A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169514937 | ||||||
chr1:169515007
|
G | A | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6528+437C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169515007 | ||||||
chr1:169515134
|
G | T | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6528+310C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169515134 | ||||||
chr1:169515204
|
CT | C | 25 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(22): Show | 25 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.6528+239delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169515204 | ||||||
chr1:169515224
|
T | C | 1 | a0024c0066t0003g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6528+220A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169515224 | ||||||
chr1:169515314
|
T | G | 117 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(114): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.6528+130A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 24/24 | chr1 | 169515314 | ||||||
chr1:169515662
|
T | G | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.6346-36A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169515662 | ||||||
chr1:169516162
|
G | T | 141 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.6346-536C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516162 | ||||||
chr1:169516201
|
G | A | 1 | a0001c0004t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6346-575C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516201 | ||||||
chr1:169516387
|
G | A | 2 | a0005c0054t0001g0054a0005c0071t0001g0293 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6346-761C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516387 | ||||||
chr1:169516388
|
T | C | 2 | a0025c0077t0005g0213a0041c0045t0005g0075 | 2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.6346-762A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516388 | ||||||
chr1:169516443
|
A | G | 2 | a0005c0006t0001g0130a0005c0006t0001g0131 | 2 | NA18747.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.6346-817T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516443 | ||||||
chr1:169516537
|
C | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6346-911G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516537 | ||||||
chr1:169516621
|
T | A | 141 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.6346-995A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516621 | ||||||
chr1:169516783
|
T | G | 5 | a0001c0001t0002g0090a0001c0002t0002g0196a0001c0002t0002g0205others(2): Show | 5 | NA18957.hp1 NA18985.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.6346-1157A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516783 | ||||||
chr1:169516890
|
G | A | 24 | a0003c0005t0004g0151a0003c0015t0004g0040a0003c0015t0004g0088others(21): Show | 25 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.6346-1264C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516890 | ||||||
chr1:169516903
|
C | G | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6346-1277G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169516903 | ||||||
chr1:169517229
|
C | T | 2 | a0017c0037t0004g0046a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.6345+1183G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517229 | ||||||
chr1:169517243
|
T | C | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | NA18952.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.6345+1169A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517243 | ||||||
chr1:169517263
|
G | C | 91 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(88): Show | 95 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.6345+1149C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517263 | ||||||
chr1:169517391
|
T | C | 1 | a0001c0004t0010g0247 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6345+1021A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517391 | ||||||
chr1:169517403
|
G | C | 295 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(292): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.6345+1009C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517403 | ||||||
chr1:169517458
|
C | T | 1 | a0001c0002t0002g0207 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.6345+954G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517458 | ||||||
chr1:169517529
|
T | G | 117 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(114): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.6345+883A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517529 | ||||||
chr1:169517812
|
C | T | 1 | a0005c0008t0001g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6345+600G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517812 | ||||||
chr1:169517813
|
G | A | 1 | a0001c0002t0002g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6345+599C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169517813 | ||||||
chr1:169518060
|
C | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6345+352G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169518060 | ||||||
chr1:169518381
|
A | G | 1 | a0001c0074t0002g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.6345+31T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 23/24 | chr1 | 169518381 | ||||||
chr1:169518583
|
G | T | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.6194-20C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169518583 | ||||||
chr1:169518652
|
C | T | 1 | a0003c0032t0001g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6194-89G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169518652 | ||||||
chr1:169518671
|
A | G | 1 | a0014c0031t0001g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6194-108T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169518671 | ||||||
chr1:169518960
|
A | C | 1 | a0004c0050t0003g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6194-397T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169518960 | ||||||
chr1:169519054
|
C | T | 1 | a0001c0004t0010g0231 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.6194-491G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519054 | ||||||
chr1:169519140
|
C | T | 1 | a0006c0020t0005g0225 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6194-577G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519140 | ||||||
chr1:169519183
|
T | C | 2 | a0001c0002t0002g0163a0001c0002t0002g0173 | 2 | HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.6194-620A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519183 | ||||||
chr1:169519323
|
A | C | 1 | a0001c0002t0002g0169 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6194-760T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519323 | ||||||
chr1:169519426
|
T | C | 4 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6194-863A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519426 | ||||||
chr1:169519686
|
C | T | 20 | a0003c0005t0004g0151a0003c0015t0004g0040a0003c0015t0004g0088others(17): Show | 21 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.6193+834G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519686 | ||||||
chr1:169519689
|
C | T | 144 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(141): Show | 144 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.6193+831G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519689 | ||||||
chr1:169519785
|
T | A | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.6193+735A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519785 | ||||||
chr1:169519803
|
T | C | 1 | a0003c0032t0004g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6193+717A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519803 | ||||||
chr1:169519915
|
A | G | 1 | a0005c0006t0001g0093 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6193+605T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519915 | ||||||
chr1:169519965
|
A | G | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.6193+555T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169519965 | ||||||
chr1:169520120
|
T | C | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.6193+400A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169520120 | ||||||
chr1:169520171
|
G | T | 2 | a0005c0006t0001g0093a0005c0008t0001g0209 | 2 | NA18947.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.6193+349C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169520171 | ||||||
chr1:169520251
|
C | G | 22 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(19): Show | 22 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.6193+269G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169520251 | ||||||
chr1:169520274
|
A | G | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.6193+246T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169520274 | ||||||
chr1:169520347
|
T | C | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.6193+173A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169520347 | ||||||
chr1:169520484
|
G | A | 5 | a0007c0041t0008g0017a0007c0056t0008g0290a0017c0037t0004g0046others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.6193+36C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 22/24 | chr1 | 169520484 | ||||||
chr1:169520708
|
A | G | 71 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(68): Show | 71 | HG00438.hp1 HG00673.hp1 HG01496.hp2 others(68): Show |
intron_variant | MODIFIER | c.6049-44T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169520708 | ||||||
chr1:169520722
|
T | A | 1 | a0005c0006t0001g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6049-58A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169520722 | ||||||
chr1:169520881
|
T | G | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0037c0046t0008g0291 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.6049-217A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169520881 | ||||||
chr1:169521119
|
G | A | 1 | a0022c0058t0003g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6049-455C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521119 | ||||||
chr1:169521154
|
G | C | 295 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(292): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.6049-490C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521154 | ||||||
chr1:169521163
|
T | C | 286 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.6049-499A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521163 | ||||||
chr1:169521354
|
A | G | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.6049-690T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521354 | ||||||
chr1:169521363
|
G | T | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6049-699C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521363 | ||||||
chr1:169521432
|
G | A | 2 | a0002c0003t0001g0253a0002c0003t0001g0254 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.6049-768C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521432 | ||||||
chr1:169521493
|
G | A | 1 | a0001c0004t0002g0239 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6049-829C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521493 | ||||||
chr1:169521518
|
A | G | 1 | a0002c0003t0001g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6049-854T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521518 | ||||||
chr1:169521534
|
G | A | 135 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(132): Show | 136 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.6049-870C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521534 | ||||||
chr1:169521549
|
C | T | 1 | a0005c0006t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6049-885G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521549 | ||||||
chr1:169521614
|
GATT | G | 3 | a0001c0001t0002g0090a0001c0002t0002g0196a0001c0074t0002g0120 | 3 | NA18957.hp1 NA19001.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.6049-953_6049-951d others(5): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521614 | ||||||
chr1:169521615
|
A | ATTTT | 61 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(58): Show | 65 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.6049-955_6049-952d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521615 | ||||||
chr1:169521615
|
A | ATTTTT | 20 | a0002c0003t0001g0015a0002c0003t0001g0220a0002c0003t0001g0238others(17): Show | 20 | HG00423.hp2 HG00735.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.6049-956_6049-952d others(7): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521615 | ||||||
chr1:169521615
|
AT | A | 14 | a0001c0001t0002g0113a0001c0001t0002g0128a0001c0001t0002g0135others(11): Show | 14 | HG02040.hp1 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.6049-952delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521615 | ||||||
chr1:169521615
|
ATT | A | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0092others(127): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.6049-953_6049-952d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521615 | ||||||
chr1:169521615
|
ATTT | A | 33 | a0001c0004t0002g0240a0003c0005t0003g0156a0003c0005t0004g0151others(30): Show | 34 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.6049-954_6049-952d others(5): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521615 | ||||||
chr1:169521615
|
ATTTT | A | 21 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(18): Show | 21 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.6049-955_6049-952d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521615 | ||||||
chr1:169521630
|
T | G | 6 | a0004c0021t0001g0221a0004c0050t0003g0279a0004c0059t0001g0300others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049-966A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521630 | ||||||
chr1:169521634
|
T | G | 36 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.6049-970A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521634 | ||||||
chr1:169521658
|
G | A | 1 | a0003c0022t0004g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6049-994C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521658 | ||||||
chr1:169521783
|
A | AT | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.6049-1120dupA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521783 | ||||||
chr1:169521810
|
G | A | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0037c0046t0008g0291 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.6049-1146C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521810 | ||||||
chr1:169521855
|
G | C | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6049-1191C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521855 | ||||||
chr1:169521870
|
C | T | 1 | a0003c0015t0014g0085 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6049-1206G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521870 | ||||||
chr1:169521871
|
G | A | 1 | a0007c0041t0006g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6049-1207C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521871 | ||||||
chr1:169521911
|
G | A | 83 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.6049-1247C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521911 | ||||||
chr1:169521925
|
AT | A | 107 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.6049-1262delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521925 | ||||||
chr1:169521941
|
C | A | 23 | a0003c0005t0004g0151a0003c0015t0004g0040a0003c0015t0004g0088others(20): Show | 24 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.6048+1256G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169521941 | ||||||
chr1:169522014
|
T | A | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6048+1183A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522014 | ||||||
chr1:169522039
|
G | A | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6048+1158C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522039 | ||||||
chr1:169522093
|
C | G | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.6048+1104G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522093 | ||||||
chr1:169522096
|
G | GTTAATTG others(15): Show |
2 | a0032c0060t0005g0297a0034c0072t0005g0292 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6048+1079_6048+110 others(26): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522096 | ||||||
chr1:169522108
|
A | G | 1 | a0004c0021t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6048+1089T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522108 | ||||||
chr1:169522317
|
G | A | 295 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(292): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.6048+880C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522317 | ||||||
chr1:169522551
|
G | T | 1 | a0022c0058t0003g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6048+646C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522551 | ||||||
chr1:169522561
|
T | G | 4 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6048+636A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522561 | ||||||
chr1:169522593
|
G | T | 1 | a0002c0003t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6048+604C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522593 | ||||||
chr1:169522861
|
A | G | 1 | a0009c0016t0003g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6048+336T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522861 | ||||||
chr1:169522862
|
T | C | 65 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(62): Show | 65 | HG00438.hp1 HG00673.hp1 HG01496.hp2 others(62): Show |
intron_variant | MODIFIER | c.6048+335A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522862 | ||||||
chr1:169522885
|
C | T | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.6048+312G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522885 | ||||||
chr1:169522998
|
G | A | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0037c0046t0008g0291 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.6048+199C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169522998 | ||||||
chr1:169523012
|
CTCTT | C | 85 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(82): Show | 85 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(82): Show |
intron_variant | MODIFIER | c.6048+181_6048+184d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169523012 | ||||||
chr1:169523118
|
C | T | 2 | a0005c0011t0001g0269a0005c0011t0001g0296 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.6048+79G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169523118 | ||||||
chr1:169523130
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.6048+67C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 21/24 | chr1 | 169523130 | ||||||
chr1:169523377
|
C | T | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5893-25G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 20/24 | chr1 | 169523377 | ||||||
chr1:169523438
|
C | T | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.5893-86G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 20/24 | chr1 | 169523438 | ||||||
chr1:169523501
|
A | G | 2 | a0032c0060t0005g0297a0034c0072t0005g0292 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5893-149T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 20/24 | chr1 | 169523501 | ||||||
chr1:169524381
|
T | G | 1 | a0007c0013t0006g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5788+456A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524381 | ||||||
chr1:169524475
|
C | T | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.5788+362G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524475 | ||||||
chr1:169524488
|
G | C | 58 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.5788+349C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524488 | ||||||
chr1:169524495
|
A | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5788+342T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524495 | ||||||
chr1:169524641
|
G | C | 2 | a0032c0060t0005g0297a0034c0072t0005g0292 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5788+196C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524641 | ||||||
chr1:169524657
|
A | G | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.5788+180T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524657 | ||||||
chr1:169524715
|
A | C | 58 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.5788+122T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 19/24 | chr1 | 169524715 | ||||||
chr1:169524958
|
C | T | 199 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(196): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.5717-50G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169524958 | ||||||
chr1:169524994
|
C | A | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0037c0046t0008g0291 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5717-86G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169524994 | ||||||
chr1:169525146
|
T | C | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.5717-238A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525146 | ||||||
chr1:169525153
|
A | T | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5717-245T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525153 | ||||||
chr1:169525165
|
T | C | 87 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(84): Show | 87 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(84): Show |
intron_variant | MODIFIER | c.5717-257A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525165 | ||||||
chr1:169525262
|
C | T | 23 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.5717-354G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525262 | ||||||
chr1:169525263
|
G | A | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.5717-355C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525263 | ||||||
chr1:169525268
|
G | A | 1 | a0002c0003t0004g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5717-360C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525268 | ||||||
chr1:169525351
|
GA | G | 4 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5717-444delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525351 | ||||||
chr1:169525504
|
T | C | 1 | a0004c0040t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5716+397A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525504 | ||||||
chr1:169525570
|
A | G | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.5716+331T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525570 | ||||||
chr1:169525758
|
G | A | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5716+143C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 18/24 | chr1 | 169525758 | ||||||
chr1:169526131
|
T | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5600-114A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526131 | ||||||
chr1:169526195
|
T | C | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.5600-178A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526195 | ||||||
chr1:169526331
|
G | C | 5 | a0007c0013t0002g0077a0007c0013t0002g0278a0007c0013t0002g0282others(2): Show | 5 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5600-314C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526331 | ||||||
chr1:169526403
|
T | G | 1 | a0003c0005t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5600-386A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526403 | ||||||
chr1:169526413
|
A | G | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0037c0046t0008g0291 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5600-396T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526413 | ||||||
chr1:169526429
|
A | G | 1 | a0004c0025t0003g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5600-412T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526429 | ||||||
chr1:169526712
|
GT | G | 9 | a0001c0001t0002g0103a0001c0001t0002g0129a0001c0001t0002g0134others(6): Show | 9 | HG02155.hp1 HG02155.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.5600-696delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526712 | ||||||
chr1:169526852
|
A | G | 1 | a0003c0032t0004g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5600-835T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526852 | ||||||
chr1:169526947
|
T | G | 4 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5600-930A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526947 | ||||||
chr1:169526973
|
T | C | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5599+942A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169526973 | ||||||
chr1:169527015
|
C | T | 59 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.5599+900G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527015 | ||||||
chr1:169527133
|
T | C | 2 | a0032c0060t0005g0297a0034c0072t0005g0292 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5599+782A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527133 | ||||||
chr1:169527343
|
A | G | 2 | a0002c0029t0001g0175a0002c0029t0001g0182 | 2 | NA18991.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.5599+572T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527343 | ||||||
chr1:169527363
|
T | C | 1 | a0003c0022t0004g0229 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5599+552A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527363 | ||||||
chr1:169527438
|
T | A | 1 | a0007c0041t0006g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5599+477A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527438 | ||||||
chr1:169527528
|
C | T | 2 | a0007c0027t0006g0271a0007c0027t0006g0272 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5599+387G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527528 | ||||||
chr1:169527562
|
C | T | 1 | a0007c0013t0002g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5599+353G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527562 | ||||||
chr1:169527644
|
C | T | 2 | a0001c0001t0002g0141a0001c0002t0002g0212 | 2 | NA18987.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.5599+271G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 17/24 | chr1 | 169527644 | ||||||
chr1:169528353
|
C | G | 1 | a0003c0005t0003g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5420-259G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528353 | ||||||
chr1:169528376
|
C | T | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.5420-282G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528376 | ||||||
chr1:169528390
|
G | C | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0037c0046t0008g0291 | 3 | HG02280.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5420-296C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528390 | ||||||
chr1:169528493
|
T | G | 87 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(84): Show | 87 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(84): Show |
intron_variant | MODIFIER | c.5420-399A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528493 | ||||||
chr1:169528582
|
G | A | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.5420-488C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528582 | ||||||
chr1:169528588
|
G | A | 1 | a0003c0032t0004g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5420-494C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528588 | ||||||
chr1:169528611
|
A | G | 7 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.5420-517T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528611 | ||||||
chr1:169528688
|
T | G | 93 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(90): Show | 93 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(90): Show |
intron_variant | MODIFIER | c.5420-594A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528688 | ||||||
chr1:169528720
|
T | A | 7 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.5420-626A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528720 | ||||||
chr1:169528772
|
A | T | 1 | a0002c0003t0001g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5420-678T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528772 | ||||||
chr1:169528818
|
A | G | 295 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(292): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.5420-724T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528818 | ||||||
chr1:169528936
|
T | G | 1 | a0008c0042t0001g0164 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5419+672A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528936 | ||||||
chr1:169528943
|
C | T | 83 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.5419+665G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528943 | ||||||
chr1:169528991
|
C | T | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5419+617G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169528991 | ||||||
chr1:169529001
|
T | C | 2 | a0005c0008t0001g0165a0005c0008t0001g0171 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.5419+607A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529001 | ||||||
chr1:169529122
|
A | G | 70 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(67): Show | 70 | HG00438.hp1 HG00673.hp1 HG01496.hp2 others(67): Show |
intron_variant | MODIFIER | c.5419+486T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529122 | ||||||
chr1:169529176
|
G | A | 3 | a0004c0007t0003g0021a0004c0007t0003g0022a0036c0061t0003g0083 | 3 | HG02293.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5419+432C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529176 | ||||||
chr1:169529180
|
G | C | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5419+428C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529180 | ||||||
chr1:169529195
|
G | A | 9 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.5419+413C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529195 | ||||||
chr1:169529596
|
T | C | 287 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(284): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.5419+12A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529596 | ||||||
chr1:169529597
|
G | A | 85 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(82): Show | 85 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(82): Show |
intron_variant | MODIFIER | c.5419+11C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 16/24 | chr1 | 169529597 | ||||||
chr1:169529952
|
A | G | 198 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(195): Show | 202 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.5209-134T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169529952 | ||||||
chr1:169529993
|
A | G | 1 | a0003c0015t0014g0085 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5209-175T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169529993 | ||||||
chr1:169530013
|
T | C | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5209-195A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530013 | ||||||
chr1:169530143
|
A | C | 83 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.5209-325T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530143 | ||||||
chr1:169530385
|
A | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5208+401T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530385 | ||||||
chr1:169530421
|
T | A | 197 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(194): Show | 201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.5208+365A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530421 | ||||||
chr1:169530457
|
T | C | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.5208+329A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530457 | ||||||
chr1:169530472
|
A | G | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5208+314T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530472 | ||||||
chr1:169530713
|
C | T | 83 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.5208+73G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 15/24 | chr1 | 169530713 | ||||||
chr1:169531110
|
G | A | 83 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.4972-88C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531110 | ||||||
chr1:169531120
|
C | A | 2 | a0004c0007t0003g0012a0009c0016t0003g0065 | 2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4972-98G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531120 | ||||||
chr1:169531243
|
G | A | 23 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.4972-221C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531243 | ||||||
chr1:169531244
|
CT | C | 7 | a0007c0013t0006g0283a0007c0027t0006g0271a0007c0027t0006g0272others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4972-223delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531244 | ||||||
chr1:169531352
|
C | A | 286 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.4972-330G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531352 | ||||||
chr1:169531506
|
T | C | 3 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0199 | 3 | NA18963.hp2 NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.4972-484A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531506 | ||||||
chr1:169531530
|
A | G | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4972-508T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531530 | ||||||
chr1:169531691
|
C | G | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.4972-669G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531691 | ||||||
chr1:169531816
|
A | T | 13 | a0004c0040t0002g0301a0004c0067t0002g0276a0010c0012t0002g0037others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.4972-794T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531816 | ||||||
chr1:169531818
|
T | C | 109 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(106): Show | 113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.4972-796A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531818 | ||||||
chr1:169531831
|
G | C | 2 | a0002c0019t0001g0284a0002c0070t0001g0277 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4972-809C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169531831 | ||||||
chr1:169532006
|
A | G | 1 | a0001c0002t0002g0161 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4972-984T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532006 | ||||||
chr1:169532188
|
G | A | 1 | a0034c0072t0005g0292 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4972-1166C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532188 | ||||||
chr1:169532274
|
G | A | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4972-1252C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532274 | ||||||
chr1:169532331
|
C | A | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.4972-1309G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532331 | ||||||
chr1:169532462
|
A | G | 85 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(82): Show | 85 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(82): Show |
intron_variant | MODIFIER | c.4972-1440T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532462 | ||||||
chr1:169532630
|
C | CCACA | 197 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(194): Show | 201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.4972-1612_4972-160 others(8): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532630 | ||||||
chr1:169532757
|
G | A | 46 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(43): Show | 47 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.4972-1735C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532757 | ||||||
chr1:169532794
|
C | T | 22 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4972-1772G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532794 | ||||||
chr1:169532901
|
A | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4972-1879T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169532901 | ||||||
chr1:169533165
|
A | G | 22 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4972-2143T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533165 | ||||||
chr1:169533181
|
C | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0105 | 2 | NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.4972-2159G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533181 | ||||||
chr1:169533216
|
C | T | 1 | a0006c0020t0005g0223 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4972-2194G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533216 | ||||||
chr1:169533258
|
A | T | 1 | a0007c0013t0002g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4972-2236T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533258 | ||||||
chr1:169533295
|
A | C | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.4972-2273T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533295 | ||||||
chr1:169533668
|
A | G | 1 | a0008c0042t0001g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4972-2646T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533668 | ||||||
chr1:169533704
|
C | T | 2 | a0007c0041t0008g0017a0007c0056t0008g0290 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4972-2682G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533704 | ||||||
chr1:169533723
|
A | G | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4972-2701T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169533723 | ||||||
chr1:169534010
|
G | A | 1 | a0005c0008t0001g0192 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4971+2496C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534010 | ||||||
chr1:169534021
|
G | A | 2 | a0009c0016t0003g0071a0028c0065t0003g0260 | 2 | HG02004.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4971+2485C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534021 | ||||||
chr1:169534102
|
C | G | 2 | a0005c0006t0001g0118a0005c0006t0001g0119 | 2 | NA18956.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4971+2404G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534102 | ||||||
chr1:169534222
|
C | T | 2 | a0012c0024t0007g0067a0012c0024t0007g0072 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4971+2284G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534222 | ||||||
chr1:169534258
|
C | T | 4 | a0003c0005t0003g0156a0003c0005t0003g0214a0003c0018t0003g0026others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.4971+2248G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534258 | ||||||
chr1:169534378
|
A | C | 85 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(82): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.4971+2128T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534378 | ||||||
chr1:169534412
|
A | C | 86 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(83): Show | 86 | HG00438.hp1 HG00673.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.4971+2094T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534412 | ||||||
chr1:169534623
|
A | G | 1 | a0003c0018t0003g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4971+1883T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534623 | ||||||
chr1:169534740
|
T | C | 3 | a0004c0069t0001g0288a0009c0030t0001g0038a0009c0030t0001g0059 | 3 | HG02486.hp1 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4971+1766A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534740 | ||||||
chr1:169534777
|
A | G | 1 | a0001c0001t0002g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4971+1729T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534777 | ||||||
chr1:169534897
|
T | C | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4971+1609A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169534897 | ||||||
chr1:169535016
|
T | C | 1 | a0002c0010t0001g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4971+1490A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535016 | ||||||
chr1:169535081
|
A | G | 1 | a0026c0051t0002g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4971+1425T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535081 | ||||||
chr1:169535083
|
G | T | 25 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(22): Show | 25 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.4971+1423C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535083 | ||||||
chr1:169535084
|
C | T | 24 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.4971+1422G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535084 | ||||||
chr1:169535165
|
C | T | 2 | a0002c0010t0001g0181a0002c0010t0001g0183 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4971+1341G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535165 | ||||||
chr1:169535497
|
G | A | 2 | a0002c0003t0001g0253a0002c0003t0001g0254 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4971+1009C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535497 | ||||||
chr1:169535591
|
C | T | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.4971+915G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535591 | ||||||
chr1:169535624
|
A | C | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4971+882T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535624 | ||||||
chr1:169535832
|
T | C | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4971+674A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535832 | ||||||
chr1:169535869
|
A | T | 1 | a0009c0016t0003g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4971+637T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535869 | ||||||
chr1:169535920
|
T | C | 198 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(195): Show | 202 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.4971+586A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535920 | ||||||
chr1:169535927
|
G | A | 1 | a0003c0026t0004g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4971+579C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535927 | ||||||
chr1:169535932
|
G | A | 1 | a0003c0005t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4971+574C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169535932 | ||||||
chr1:169536057
|
A | G | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4971+449T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169536057 | ||||||
chr1:169536260
|
A | G | 2 | a0003c0005t0003g0214a0003c0018t0003g0026 | 2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.4971+246T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169536260 | ||||||
chr1:169536292
|
T | C | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4971+214A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169536292 | ||||||
chr1:169536319
|
CT | C | 98 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(95): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.4971+186delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169536319 | ||||||
chr1:169536409
|
C | A | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4971+97G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 14/24 | chr1 | 169536409 | ||||||
chr1:169537003
|
A | G | 110 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(107): Show | 114 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.4797-323T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169537003 | ||||||
chr1:169537402
|
T | C | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4797-722A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169537402 | ||||||
chr1:169537453
|
G | A | 1 | a0004c0023t0003g0198 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4797-773C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169537453 | ||||||
chr1:169537772
|
C | T | 23 | a0003c0005t0004g0151a0003c0015t0004g0040a0003c0015t0004g0088others(20): Show | 24 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.4797-1092G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169537772 | ||||||
chr1:169537838
|
T | A | 86 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(83): Show | 90 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.4797-1158A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169537838 | ||||||
chr1:169538092
|
A | T | 1 | a0004c0059t0001g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4797-1412T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538092 | ||||||
chr1:169538244
|
T | A | 1 | a0003c0005t0003g0027 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4797-1564A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538244 | ||||||
chr1:169538394
|
G | T | 8 | a0010c0012t0002g0050a0010c0012t0002g0061a0010c0012t0002g0062others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.4797-1714C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538394 | ||||||
chr1:169538576
|
G | A | 1 | a0001c0002t0002g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4796+1718C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538576 | ||||||
chr1:169538595
|
C | A | 1 | a0003c0032t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4796+1699G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538595 | ||||||
chr1:169538606
|
G | T | 108 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(105): Show | 112 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.4796+1688C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538606 | ||||||
chr1:169538666
|
G | A | 2 | a0022c0058t0003g0299a0042c0043t0003g0010 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4796+1628C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538666 | ||||||
chr1:169538744
|
T | C | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.4796+1550A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169538744 | ||||||
chr1:169539199
|
C | T | 2 | a0007c0041t0008g0017a0007c0056t0008g0290 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4796+1095G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539199 | ||||||
chr1:169539211
|
A | C | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4796+1083T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539211 | ||||||
chr1:169539336
|
G | A | 2 | a0022c0058t0003g0299a0042c0043t0003g0010 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4796+958C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539336 | ||||||
chr1:169539338
|
A | C | 194 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(191): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.4796+956T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539338 | ||||||
chr1:169539376
|
A | T | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4796+918T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539376 | ||||||
chr1:169539467
|
AGTT | A | 29 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.4796+824_4796+826d others(5): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539467 | ||||||
chr1:169539501
|
A | T | 85 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(82): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.4796+793T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539501 | ||||||
chr1:169539553
|
T | A | 1 | a0006c0009t0005g0107 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4796+741A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539553 | ||||||
chr1:169539702
|
T | C | 3 | a0007c0041t0008g0017a0007c0056t0008g0290a0039c0048t0016g0073 | 3 | HG02922.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4796+592A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539702 | ||||||
chr1:169539703
|
G | A | 2 | a0011c0017t0004g0066a0011c0017t0004g0068 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4796+591C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539703 | ||||||
chr1:169539801
|
A | G | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4796+493T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539801 | ||||||
chr1:169539925
|
A | G | 196 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(193): Show | 200 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.4796+369T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169539925 | ||||||
chr1:169540202
|
A | G | 1 | a0034c0072t0005g0292 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4796+92T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169540202 | ||||||
chr1:169540245
|
T | G | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.4796+49A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 13/24 | chr1 | 169540245 | ||||||
chr1:169543259
|
C | A | 85 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(82): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1976-145G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543259 | ||||||
chr1:169543260
|
C | T | 1 | a0002c0003t0004g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1976-146G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543260 | ||||||
chr1:169543286
|
C | T | 196 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(193): Show | 200 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1976-172G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543286 | ||||||
chr1:169543324
|
T | C | 85 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(82): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1976-210A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543324 | ||||||
chr1:169543356
|
G | A | 84 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1976-242C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543356 | ||||||
chr1:169543405
|
A | C | 205 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(202): Show | 209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1976-291T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543405 | ||||||
chr1:169543413
|
G | A | 85 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(82): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1976-299C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543413 | ||||||
chr1:169543430
|
A | G | 2 | a0033c0080t0017g0215a0034c0072t0005g0292 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1976-316T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543430 | ||||||
chr1:169543442
|
AG | A | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1976-329delC | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543442 | ||||||
chr1:169543601
|
C | T | 23 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1976-487G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543601 | ||||||
chr1:169543675
|
C | T | 85 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(82): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1976-561G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543675 | ||||||
chr1:169543742
|
G | A | 110 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(107): Show | 114 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1975+554C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543742 | ||||||
chr1:169543892
|
C | T | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1975+404G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169543892 | ||||||
chr1:169544198
|
C | A | 83 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1975+98G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 12/24 | chr1 | 169544198 | ||||||
chr1:169544702
|
A | G | 3 | a0004c0023t0003g0155a0004c0023t0003g0186a0004c0023t0003g0198 | 3 | HG01069.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1763-194T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169544702 | ||||||
chr1:169544768
|
A | G | 286 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.1763-260T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169544768 | ||||||
chr1:169545099
|
A | G | 98 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(95): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1763-591T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545099 | ||||||
chr1:169545117
|
G | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1763-609C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545117 | ||||||
chr1:169545270
|
C | T | 5 | a0007c0013t0002g0077a0007c0013t0002g0278a0007c0013t0002g0282others(2): Show | 5 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1763-762G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545270 | ||||||
chr1:169545310
|
G | A | 83 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(80): Show | 83 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1763-802C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545310 | ||||||
chr1:169545541
|
G | A | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1762+901C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545541 | ||||||
chr1:169545552
|
G | A | 23 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0224others(20): Show | 25 | HG00099.hp1 HG01074.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1762+890C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545552 | ||||||
chr1:169545692
|
A | G | 35 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1762+750T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545692 | ||||||
chr1:169545701
|
A | G | 1 | a0022c0058t0003g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1762+741T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545701 | ||||||
chr1:169545745
|
A | G | 1 | a0001c0002t0002g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1762+697T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545745 | ||||||
chr1:169545775
|
C | T | 2 | a0002c0019t0001g0284a0002c0070t0001g0277 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1762+667G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545775 | ||||||
chr1:169545812
|
T | C | 1 | a0005c0011t0009g0001 | 2 | HG00738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1762+630A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545812 | ||||||
chr1:169545945
|
A | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1762+497T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545945 | ||||||
chr1:169545958
|
A | T | 2 | a0007c0041t0008g0017a0007c0056t0008g0290 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1762+484T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545958 | ||||||
chr1:169545966
|
T | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1762+476A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169545966 | ||||||
chr1:169546058
|
C | G | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1762+384G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546058 | ||||||
chr1:169546069
|
A | G | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1762+373T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546069 | ||||||
chr1:169546120
|
A | G | 1 | a0009c0016t0003g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1762+322T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546120 | ||||||
chr1:169546143
|
T | C | 200 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(197): Show | 204 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1762+299A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546143 | ||||||
chr1:169546180
|
T | TAC | 10 | a0001c0001t0002g0141a0001c0002t0002g0189a0001c0002t0002g0205others(7): Show | 10 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+260_1762+261d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546180 | ||||||
chr1:169546180
|
TAC | T | 36 | a0003c0015t0004g0040a0003c0015t0004g0088a0003c0015t0004g0089others(33): Show | 37 | HG00438.hp2 HG00733.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1762+260_1762+261d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546180 | ||||||
chr1:169546180
|
TACAC | T | 25 | a0003c0005t0003g0214a0006c0009t0005g0055a0006c0009t0005g0078others(22): Show | 25 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1762+258_1762+261d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546180 | ||||||
chr1:169546205
|
A | G | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1762+237T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546205 | ||||||
chr1:169546208
|
C | CACAT | 3 | a0002c0003t0001g0220a0014c0031t0001g0052a0030c0055t0011g0076 | 3 | HG02818.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1762+233_1762+234i others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546208 | ||||||
chr1:169546208
|
C | CAT | 73 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(70): Show | 77 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1762+233_1762+234i others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546208 | ||||||
chr1:169546208
|
C | T | 1 | a0005c0006t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1762+234G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546208 | ||||||
chr1:169546291
|
C | T | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1762+151G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546291 | ||||||
chr1:169546298
|
C | T | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1762+144G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546298 | ||||||
chr1:169546420
|
C | A | 1 | a0003c0005t0003g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1762+22G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 11/24 | chr1 | 169546420 | ||||||
chr1:169546636
|
T | A | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1612-44A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546636 | ||||||
chr1:169546678
|
G | A | 72 | a0002c0003t0001g0003a0002c0003t0001g0013a0002c0003t0001g0015others(69): Show | 75 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1612-86C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546678 | ||||||
chr1:169546687
|
A | G | 23 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1612-95T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546687 | ||||||
chr1:169546698
|
T | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1612-106A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546698 | ||||||
chr1:169546857
|
C | T | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1612-265G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546857 | ||||||
chr1:169546901
|
G | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1612-309C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546901 | ||||||
chr1:169546966
|
T | TA | 6 | a0012c0024t0007g0067a0012c0024t0007g0072a0012c0024t0012g0044others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1612-375dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546966 | ||||||
chr1:169546966
|
TA | T | 38 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.1612-375delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546966 | ||||||
chr1:169546966
|
TAA | T | 22 | a0004c0025t0003g0126a0006c0009t0005g0055a0006c0009t0005g0078others(19): Show | 22 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1612-376_1612-375d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546966 | ||||||
chr1:169546977
|
AAAAAAAG | A | 75 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(72): Show | 79 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1612-392_1612-386d others(9): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546977 | ||||||
chr1:169546978
|
AAAAAAGA others(4): Show |
A | 95 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(92): Show | 95 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1612-397_1612-387d others(13): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546978 | ||||||
chr1:169546985
|
A | G | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1612-393T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169546985 | ||||||
chr1:169547030
|
T | G | 94 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(91): Show | 94 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1612-438A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547030 | ||||||
chr1:169547051
|
G | A | 1 | a0006c0009t0005g0082 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1612-459C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547051 | ||||||
chr1:169547121
|
G | A | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1612-529C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547121 | ||||||
chr1:169547135
|
C | T | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1612-543G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547135 | ||||||
chr1:169547152
|
C | T | 21 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1612-560G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547152 | ||||||
chr1:169547206
|
C | A | 1 | a0005c0008t0001g0168 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1612-614G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547206 | ||||||
chr1:169547269
|
G | A | 111 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(108): Show | 111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1612-677C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547269 | ||||||
chr1:169547438
|
A | C | 1 | a0002c0019t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1612-846T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547438 | ||||||
chr1:169547462
|
G | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1612-870C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547462 | ||||||
chr1:169547523
|
G | A | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1612-931C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547523 | ||||||
chr1:169547528
|
G | T | 2 | a0033c0080t0017g0215a0034c0072t0005g0292 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1612-936C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547528 | ||||||
chr1:169547753
|
T | A | 3 | a0004c0069t0001g0288a0009c0030t0001g0038a0009c0030t0001g0059 | 3 | HG02486.hp1 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1612-1161A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547753 | ||||||
chr1:169547838
|
T | C | 1 | a0005c0008t0001g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1612-1246A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547838 | ||||||
chr1:169547921
|
C | T | 110 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1612-1329G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547921 | ||||||
chr1:169547986
|
T | A | 3 | a0002c0003t0001g0224a0002c0010t0001g0181a0002c0010t0001g0183 | 3 | HG01243.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1612-1394A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169547986 | ||||||
chr1:169548102
|
A | G | 1 | a0006c0009t0005g0082 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1612-1510T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548102 | ||||||
chr1:169548147
|
A | G | 110 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1612-1555T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548147 | ||||||
chr1:169548385
|
C | G | 1 | a0001c0001t0002g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1611+1416G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548385 | ||||||
chr1:169548590
|
G | A | 4 | a0012c0024t0007g0047a0012c0024t0007g0067a0012c0024t0007g0072others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1611+1211C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548590 | ||||||
chr1:169548595
|
C | G | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1611+1206G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548595 | ||||||
chr1:169548666
|
G | A | 105 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1611+1135C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548666 | ||||||
chr1:169548672
|
A | G | 21 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1611+1129T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548672 | ||||||
chr1:169548685
|
T | C | 1 | a0001c0002t0002g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1611+1116A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548685 | ||||||
chr1:169548693
|
C | T | 21 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1611+1108G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548693 | ||||||
chr1:169548737
|
C | T | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1611+1064G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548737 | ||||||
chr1:169548742
|
G | A | 8 | a0007c0041t0008g0017a0007c0056t0008g0290a0016c0035t0004g0069others(5): Show | 8 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1611+1059C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548742 | ||||||
chr1:169548843
|
T | C | 1 | a0010c0012t0002g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1611+958A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548843 | ||||||
chr1:169548873
|
GA | G | 96 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(93): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1611+927delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548873 | ||||||
chr1:169548890
|
C | A | 2 | a0004c0007t0003g0012a0009c0016t0003g0065 | 2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1611+911G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169548890 | ||||||
chr1:169549084
|
T | G | 21 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1611+717A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549084 | ||||||
chr1:169549433
|
C | A | 1 | a0002c0003t0001g0238 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1611+368G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549433 | ||||||
chr1:169549465
|
T | C | 110 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1611+336A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549465 | ||||||
chr1:169549537
|
A | G | 34 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1611+264T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549537 | ||||||
chr1:169549549
|
C | T | 1 | a0002c0003t0001g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1611+252G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549549 | ||||||
chr1:169549581
|
TCA | T | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1611+218_1611+219d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549581 | ||||||
chr1:169549617
|
G | A | 2 | a0033c0080t0017g0215a0034c0072t0005g0292 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1611+184C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549617 | ||||||
chr1:169549634
|
C | CA | 20 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1611+166dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549634 | ||||||
chr1:169549634
|
CA | C | 224 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(221): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1611+166delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 10/24 | chr1 | 169549634 | ||||||
chr1:169550066
|
A | G | 1 | a0003c0018t0003g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1397-51T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550066 | ||||||
chr1:169550179
|
G | A | 137 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1397-164C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550179 | ||||||
chr1:169550188
|
T | A | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1397-173A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550188 | ||||||
chr1:169550270
|
T | C | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1397-255A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550270 | ||||||
chr1:169550288
|
A | AC | 20 | a0001c0002t0002g0199a0003c0005t0003g0033a0003c0005t0003g0156others(17): Show | 20 | HG00423.hp2 HG00438.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1397-274dupG | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550288 | ||||||
chr1:169550288
|
A | C | 4 | a0001c0001t0002g0090a0001c0001t0002g0135a0003c0005t0003g0153others(1): Show | 4 | NA18991.hp1 NA19001.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-273T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550288 | ||||||
chr1:169550288
|
AC | A | 65 | a0001c0001t0002g0087a0001c0001t0002g0092a0001c0001t0002g0094others(62): Show | 65 | HG00438.hp1 HG01109.hp2 HG02040.hp1 others(62): Show |
intron_variant | MODIFIER | c.1397-274delG | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550288 | ||||||
chr1:169550288
|
ACCCC | A | 75 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(72): Show | 79 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1397-277_1397-274d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550288 | ||||||
chr1:169550289
|
C | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0135 | 2 | NA19001.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1397-274G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550289 | ||||||
chr1:169550291
|
C | A | 1 | a0005c0006t0001g0130 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1397-276G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550291 | ||||||
chr1:169550294
|
C | T | 2 | a0033c0080t0017g0215a0034c0072t0005g0292 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1397-279G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550294 | ||||||
chr1:169550295
|
C | G | 3 | a0003c0015t0004g0040a0003c0022t0004g0241a0003c0032t0001g0179 | 3 | HG01952.hp1 HG02735.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1397-280G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550295 | ||||||
chr1:169550297
|
C | A | 2 | a0007c0027t0015g0274a0010c0012t0002g0062 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1397-282G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550297 | ||||||
chr1:169550299
|
C | CG | 6 | a0004c0007t0003g0246a0004c0007t0003g0266a0004c0023t0003g0152others(3): Show | 6 | HG01099.hp1 HG02602.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397-285_1397-284i others(3): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550299 | ||||||
chr1:169550299
|
C | G | 29 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1397-284G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550299 | ||||||
chr1:169550311
|
G | A | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1397-296C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550311 | ||||||
chr1:169550433
|
T | C | 19 | a0003c0015t0004g0040a0003c0015t0004g0088a0003c0015t0004g0089others(16): Show | 20 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1396+207A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550433 | ||||||
chr1:169550492
|
G | C | 1 | a0003c0022t0004g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396+148C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550492 | ||||||
chr1:169550527
|
A | G | 105 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1396+113T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 9/24 | chr1 | 169550527 | ||||||
chr1:169550754
|
C | T | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1297-15G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169550754 | ||||||
chr1:169550860
|
A | G | 213 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(210): Show | 217 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1297-121T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169550860 | ||||||
chr1:169550976
|
T | C | 1 | a0039c0048t0016g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1297-237A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169550976 | ||||||
chr1:169551000
|
C | T | 1 | a0030c0055t0011g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1297-261G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551000 | ||||||
chr1:169551093
|
C | G | 2 | a0016c0035t0004g0069a0016c0035t0004g0070 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1297-354G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551093 | ||||||
chr1:169551094
|
T | C | 2 | a0033c0080t0017g0215a0034c0072t0005g0292 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1297-355A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551094 | ||||||
chr1:169551113
|
C | A | 22 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(19): Show | 22 | HG00423.hp1 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1297-374G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551113 | ||||||
chr1:169551126
|
C | T | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1297-387G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551126 | ||||||
chr1:169551221
|
G | C | 76 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(73): Show | 80 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1297-482C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551221 | ||||||
chr1:169551222
|
G | T | 19 | a0003c0015t0004g0040a0003c0015t0004g0088a0003c0015t0004g0089others(16): Show | 20 | HG00438.hp2 HG00733.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1297-483C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551222 | ||||||
chr1:169551311
|
G | A | 76 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(73): Show | 80 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1297-572C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551311 | ||||||
chr1:169551354
|
G | A | 77 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(74): Show | 81 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1297-615C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551354 | ||||||
chr1:169551355
|
T | C | 10 | a0010c0012t0002g0037a0010c0012t0002g0042a0010c0012t0002g0050others(7): Show | 10 | HG01109.hp2 HG01243.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1297-616A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551355 | ||||||
chr1:169551392
|
G | A | 2 | a0002c0003t0001g0253a0002c0003t0001g0254 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1297-653C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551392 | ||||||
chr1:169551400
|
T | C | 1 | a0024c0066t0003g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1297-661A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551400 | ||||||
chr1:169551449
|
G | T | 1 | a0003c0005t0003g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1297-710C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551449 | ||||||
chr1:169551450
|
G | A | 35 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1297-711C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551450 | ||||||
chr1:169551727
|
C | G | 1 | a0004c0040t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1296+830G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551727 | ||||||
chr1:169551755
|
A | T | 98 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(95): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1296+802T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169551755 | ||||||
chr1:169552028
|
T | C | 2 | a0009c0016t0003g0071a0028c0065t0003g0260 | 2 | HG02004.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1296+529A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169552028 | ||||||
chr1:169552079
|
A | C | 21 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1296+478T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169552079 | ||||||
chr1:169552313
|
C | G | 35 | a0004c0007t0003g0012a0004c0007t0003g0021a0004c0007t0003g0022others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1296+244G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169552313 | ||||||
chr1:169552315
|
G | A | 294 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(291): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1296+242C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169552315 | ||||||
chr1:169552462
|
G | C | 1 | a0004c0050t0003g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1296+95C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169552462 | ||||||
chr1:169552495
|
C | T | 8 | a0007c0013t0006g0283a0007c0027t0006g0271a0007c0027t0006g0272others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296+62G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 8/24 | chr1 | 169552495 | ||||||
chr1:169553044
|
G | A | 2 | a0004c0040t0002g0301a0004c0067t0002g0276 | 2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1119-310C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553044 | ||||||
chr1:169553316
|
G | T | 20 | a0003c0005t0003g0027a0003c0005t0003g0029a0003c0005t0003g0031others(17): Show | 20 | HG00423.hp1 HG00733.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1119-582C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553316 | ||||||
chr1:169553393
|
T | A | 106 | a0002c0003t0001g0003a0002c0003t0001g0005a0002c0003t0001g0013others(103): Show | 110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1119-659A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553393 | ||||||
chr1:169553425
|
G | A | 1 | a0006c0076t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1119-691C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553425 | ||||||
chr1:169553435
|
G | A | 1 | a0006c0076t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1119-701C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553435 | ||||||
chr1:169553489
|
A | G | 1 | a0003c0022t0004g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1119-755T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553489 | ||||||
chr1:169553503
|
T | C | 1 | a0032c0060t0005g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1119-769A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553503 | ||||||
chr1:169553513
|
C | A | 7 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119-779G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553513 | ||||||
chr1:169553586
|
T | G | 1 | a0022c0058t0003g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1119-852A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553586 | ||||||
chr1:169553605
|
T | C | 3 | a0004c0050t0003g0279a0007c0027t0015g0274a0022c0058t0003g0299 | 3 | HG03453.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1119-871A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553605 | ||||||
chr1:169553678
|
C | T | 2 | a0014c0031t0001g0058a0043c0044t0001g0007 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1119-944G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553678 | ||||||
chr1:169553705
|
G | C | 65 | a0001c0001t0002g0129a0001c0001t0002g0140a0001c0002t0002g0157others(62): Show | 67 | HG00099.hp1 HG00423.hp1 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1119-971C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553705 | ||||||
chr1:169553708
|
C | A | 2 | a0022c0058t0003g0299a0039c0048t0016g0073 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1119-974G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553708 | ||||||
chr1:169553716
|
C | T | 1 | a0001c0002t0002g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1119-982G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553716 | ||||||
chr1:169553779
|
A | G | 2 | a0001c0001t0002g0128a0001c0002t0002g0028 | 2 | NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1119-1045T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553779 | ||||||
chr1:169553799
|
G | C | 60 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0002g0101others(57): Show | 60 | HG01109.hp2 HG01243.hp2 HG01255.hp2 others(57): Show |
intron_variant | MODIFIER | c.1119-1065C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553799 | ||||||
chr1:169553822
|
A | G | 3 | a0002c0003t0001g0015a0007c0041t0006g0014a0037c0046t0008g0291 | 3 | HG02280.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1119-1088T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169553822 | ||||||
chr1:169554011
|
A | T | 166 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1118+1171T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554011 | ||||||
chr1:169554098
|
A | G | 8 | a0001c0002t0002g0196a0003c0032t0004g0191a0009c0016t0003g0043others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1118+1084T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554098 | ||||||
chr1:169554108
|
A | G | 11 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0008t0001g0192others(8): Show | 11 | HG00408.hp1 HG01109.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1118+1074T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554108 | ||||||
chr1:169554124
|
T | A | 22 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0054t0001g0054others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1118+1058A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554124 | ||||||
chr1:169554124
|
T | TGAAAACT others(90): Show |
1 | a0006c0020t0005g0225 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1118+1057_1118+105 others(101): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554124 | ||||||
chr1:169554146
|
A | G | 11 | a0002c0003t0001g0013a0002c0003t0001g0015a0003c0073t0004g0039others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1118+1036T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554146 | ||||||
chr1:169554148
|
G | A | 23 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0054t0001g0054others(20): Show | 23 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1118+1034C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554148 | ||||||
chr1:169554151
|
T | C | 24 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0054t0001g0054others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1118+1031A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554151 | ||||||
chr1:169554154
|
CA | C | 24 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0054t0001g0054others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1118+1027delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554154 | ||||||
chr1:169554158
|
A | T | 24 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0054t0001g0054others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1118+1024T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554158 | ||||||
chr1:169554159
|
T | G | 24 | a0001c0002t0002g0196a0003c0032t0004g0191a0005c0054t0001g0054others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1118+1023A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554159
|
T | TGACCTCC others(88): Show |
6 | a0002c0003t0001g0220a0002c0003t0004g0275a0002c0019t0001g0284others(3): Show | 6 | HG00733.hp2 HG02559.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1118+1022_1118+102 others(99): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554159
|
T | TGACCTCC others(88): Show |
1 | a0004c0050t0003g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1118+1022_1118+102 others(99): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554159
|
T | TGACCTCC others(185): Show |
1 | a0004c0023t0003g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1118+1022_1118+102 others(196): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554159
|
T | TGACCTCC others(89): Show |
32 | a0001c0004t0002g0230a0002c0003t0001g0025a0002c0003t0001g0248others(29): Show | 34 | HG00140.hp2 HG01123.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1118+1022_1118+102 others(100): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554159
|
T | TGACCTCC others(89): Show |
1 | a0004c0021t0006g0245 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1118+1022_1118+102 others(100): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554159
|
T | TGACCTCC others(89): Show |
4 | a0005c0011t0001g0020a0005c0011t0001g0269a0005c0011t0001g0296others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1118+1022_1118+102 others(100): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554159 | ||||||
chr1:169554162
|
C | CCTCCCTA others(88): Show |
1 | a0011c0036t0003g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1118+1019_1118+102 others(99): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554162 | ||||||
chr1:169554299
|
G | A | 176 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(173): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1118+883C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554299 | ||||||
chr1:169554341
|
A | G | 105 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1118+841T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554341 | ||||||
chr1:169554377
|
G | A | 1 | a0022c0058t0003g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1118+805C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554377 | ||||||
chr1:169554401
|
G | A | 1 | a0022c0058t0003g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1118+781C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554401 | ||||||
chr1:169554464
|
T | C | 5 | a0003c0015t0004g0089a0005c0006t0001g0093a0005c0006t0001g0118others(2): Show | 5 | HG02056.hp1 NA18948.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1118+718A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554464 | ||||||
chr1:169554468
|
G | A | 115 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0002g0101others(112): Show | 118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1118+714C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554468 | ||||||
chr1:169554495
|
C | T | 1 | a0003c0018t0003g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1118+687G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554495 | ||||||
chr1:169554496
|
G | A | 1 | a0004c0007t0003g0267 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1118+686C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554496 | ||||||
chr1:169554586
|
C | T | 2 | a0014c0031t0001g0035a0040c0049t0001g0036 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1118+596G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554586 | ||||||
chr1:169554655
|
T | G | 1 | a0003c0005t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1118+527A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554655 | ||||||
chr1:169554672
|
T | A | 9 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(6): Show | 9 | HG02155.hp2 HG02258.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1118+510A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554672 | ||||||
chr1:169554676
|
T | C | 51 | a0001c0001t0002g0128a0001c0002t0002g0028a0001c0002t0002g0030others(48): Show | 51 | HG00423.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1118+506A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554676 | ||||||
chr1:169554685
|
T | G | 9 | a0010c0012t0002g0042a0010c0012t0002g0050a0010c0012t0002g0061others(6): Show | 9 | HG01109.hp2 HG01243.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1118+497A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169554685 | ||||||
chr1:169555017
|
G | C | 5 | a0004c0040t0002g0301a0004c0059t0001g0300a0021c0057t0002g0298others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1118+165C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169555017 | ||||||
chr1:169555102
|
T | G | 1 | a0004c0007t0003g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1118+80A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 7/24 | chr1 | 169555102 | ||||||
chr1:169555602
|
G | A | 18 | a0002c0070t0001g0277a0003c0022t0004g0016a0004c0040t0002g0301others(15): Show | 18 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.953-255C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555602 | ||||||
chr1:169555621
|
T | TCACTGTT others(8): Show |
124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.953-275_953-274ins others(15): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555621 | ||||||
chr1:169555623
|
T | G | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.953-276A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555623 | ||||||
chr1:169555625
|
T | A | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.953-278A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555625 | ||||||
chr1:169555630
|
T | A | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.953-283A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555630 | ||||||
chr1:169555631
|
C | G | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.953-284G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555631 | ||||||
chr1:169555633
|
T | TCAACCAT others(611): Show |
1 | a0002c0019t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.953-287_953-286ins others(618): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(608): Show |
1 | a0001c0001t0002g0128 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(615): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(609): Show |
1 | a0001c0001t0002g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(616): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(610): Show |
23 | a0001c0001t0002g0090a0001c0001t0002g0094a0001c0001t0002g0101others(20): Show | 23 | HG00423.hp2 HG01255.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.953-287_953-286ins others(617): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(611): Show |
45 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0092others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.953-287_953-286ins others(618): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(612): Show |
7 | a0009c0016t0003g0056a0009c0016t0003g0065a0009c0030t0001g0059others(4): Show | 7 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-287_953-286ins others(619): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(613): Show |
2 | a0007c0013t0002g0041a0017c0037t0004g0046 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.953-287_953-286ins others(620): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(609): Show |
1 | a0010c0012t0002g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(616): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(610): Show |
2 | a0009c0016t0003g0043a0011c0036t0003g0049 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.953-287_953-286ins others(617): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(611): Show |
14 | a0002c0019t0018g0121a0007c0013t0002g0077a0009c0016t0003g0051others(11): Show | 14 | HG01243.hp2 HG01346.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.953-287_953-286ins others(618): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(612): Show |
11 | a0002c0019t0001g0284a0004c0050t0003g0279a0007c0013t0002g0278others(8): Show | 12 | HG02280.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.953-287_953-286ins others(619): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(613): Show |
1 | a0016c0035t0004g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(620): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(611): Show |
7 | a0003c0018t0003g0026a0003c0018t0003g0048a0005c0054t0001g0054others(4): Show | 7 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-287_953-286ins others(618): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(612): Show |
3 | a0005c0006t0001g0280a0007c0013t0006g0283a0029c0052t0002g0281 | 3 | HG01884.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.953-287_953-286ins others(619): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(613): Show |
1 | a0007c0013t0002g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(620): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(611): Show |
1 | a0002c0019t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.953-287_953-286ins others(618): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(613): Show |
1 | a0007c0013t0002g0282 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(620): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(612): Show |
1 | a0012c0024t0012g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.953-287_953-286ins others(619): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555633
|
T | TCAACCAT others(611): Show |
1 | a0017c0037t0003g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.953-287_953-286ins others(618): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555633 | ||||||
chr1:169555753
|
C | T | 8 | a0002c0019t0001g0284a0004c0050t0003g0279a0005c0006t0001g0280others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-406G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555753 | ||||||
chr1:169555833
|
C | T | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.953-486G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555833 | ||||||
chr1:169555933
|
G | T | 69 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(66): Show | 69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.953-586C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555933 | ||||||
chr1:169555953
|
A | C | 1 | a0005c0008t0001g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.953-606T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169555953 | ||||||
chr1:169556011
|
A | G | 69 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(66): Show | 69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.952+635T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556011 | ||||||
chr1:169556074
|
C | T | 46 | a0002c0019t0001g0053a0003c0018t0003g0026a0003c0018t0003g0048others(43): Show | 47 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.952+572G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556074 | ||||||
chr1:169556319
|
T | TCTCTGGC | 244 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(241): Show | 245 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.952+326_952+327ins others(7): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556319 | ||||||
chr1:169556425
|
T | TAAAAAA | 7 | a0002c0003t0001g0025a0003c0015t0004g0123a0004c0067t0002g0276others(4): Show | 7 | HG01168.hp1 HG02273.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.952+215_952+220dup others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA | 64 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(61): Show | 64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+214_952+220dup others(7): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(4): Show |
5 | a0002c0019t0001g0053a0003c0018t0003g0048a0004c0040t0003g0289others(2): Show | 5 | HG00099.hp1 HG02293.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.952+210_952+220dup others(11): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(5): Show |
32 | a0001c0004t0002g0232a0001c0004t0002g0249a0002c0003t0001g0003others(29): Show | 36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.952+209_952+220dup others(12): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(6): Show |
10 | a0001c0004t0002g0230a0001c0004t0010g0247a0002c0003t0001g0262others(7): Show | 10 | HG01123.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.952+208_952+220dup others(13): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(7): Show |
71 | a0001c0002t0002g0028a0001c0002t0002g0157a0001c0002t0002g0158others(68): Show | 71 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.952+207_952+220dup others(14): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(8): Show |
25 | a0001c0002t0002g0174a0001c0002t0002g0197a0001c0002t0002g0207others(22): Show | 25 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.952+206_952+220dup others(15): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(9): Show |
6 | a0001c0002t0002g0030a0001c0002t0002g0169a0001c0002t0002g0205others(3): Show | 6 | HG01934.hp1 HG02135.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.952+205_952+220dup others(16): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(10): Show |
1 | a0016c0035t0004g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.952+220_952+221ins others(17): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(11): Show |
1 | a0021c0057t0002g0298 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.952+220_952+221ins others(18): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(12): Show |
5 | a0002c0070t0001g0277a0004c0059t0001g0300a0010c0012t0002g0061others(2): Show | 5 | HG02622.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(19): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(13): Show |
7 | a0002c0003t0001g0013a0002c0003t0001g0015a0007c0041t0006g0014others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(20): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(15): Show |
3 | a0010c0012t0002g0042a0018c0033t0006g0008a0019c0034t0002g0006 | 3 | HG02280.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+220_952+221ins others(22): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(16): Show |
4 | a0004c0040t0002g0301a0010c0012t0002g0050a0014c0031t0001g0052others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(23): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(18): Show |
4 | a0001c0004t0002g0023a0001c0004t0002g0024a0009c0016t0003g0051others(1): Show | 4 | HG01361.hp1 HG02155.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(25): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(19): Show |
1 | a0002c0003t0001g0019 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.952+220_952+221ins others(26): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(22): Show |
5 | a0004c0007t0003g0021a0007c0013t0002g0041a0014c0031t0001g0058others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(29): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(23): Show |
6 | a0003c0018t0003g0026a0004c0007t0003g0022a0005c0011t0001g0020others(3): Show | 6 | HG00738.hp2 HG01071.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(30): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(24): Show |
3 | a0006c0009t0005g0055a0006c0009t0005g0078a0007c0013t0002g0077 | 3 | HG01069.hp2 HG01433.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.952+220_952+221ins others(31): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(26): Show |
2 | a0012c0024t0007g0072a0012c0024t0012g0044 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.952+220_952+221ins others(33): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(27): Show |
6 | a0009c0016t0003g0056a0009c0016t0003g0065a0011c0017t0004g0060others(3): Show | 6 | HG01109.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.952+220_952+221ins others(34): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(28): Show |
3 | a0009c0016t0003g0043a0009c0030t0001g0059a0017c0037t0004g0046 | 3 | HG02486.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.952+220_952+221ins others(35): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(31): Show |
1 | a0016c0035t0004g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.952+220_952+221ins others(38): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(32): Show |
1 | a0017c0037t0003g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.952+220_952+221ins others(39): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556425
|
T | TAAAAAAA others(34): Show |
2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.952+220_952+221ins others(41): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556425 | ||||||
chr1:169556442
|
C | T | 1 | a0026c0051t0002g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.952+204G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556442 | ||||||
chr1:169556528
|
T | C | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.952+118A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556528 | ||||||
chr1:169556570
|
G | A | 98 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.952+76C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 6/24 | chr1 | 169556570 | ||||||
chr1:169557023
|
C | CA | 209 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(206): Show | 210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.731-157dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557023 | ||||||
chr1:169557062
|
C | T | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.731-195G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557062 | ||||||
chr1:169557129
|
A | G | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.731-262T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557129 | ||||||
chr1:169557187
|
G | T | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.731-320C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557187 | ||||||
chr1:169557192
|
G | A | 1 | a0006c0076t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.731-325C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557192 | ||||||
chr1:169557248
|
C | T | 1 | a0003c0005t0003g0029 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.731-381G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557248 | ||||||
chr1:169557363
|
G | C | 224 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(221): Show | 225 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.731-496C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557363 | ||||||
chr1:169557408
|
A | G | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.731-541T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557408 | ||||||
chr1:169557712
|
C | G | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.731-845G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557712 | ||||||
chr1:169557863
|
T | C | 10 | a0001c0002t0002g0176a0002c0010t0001g0181a0002c0010t0001g0183others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.731-996A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557863 | ||||||
chr1:169557986
|
C | T | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.731-1119G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557986 | ||||||
chr1:169557988
|
A | G | 225 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(222): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.731-1121T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169557988 | ||||||
chr1:169558089
|
A | C | 1 | a0004c0021t0006g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.730+1064T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558089 | ||||||
chr1:169558230
|
TA | T | 127 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(124): Show | 128 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.730+922delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558230 | ||||||
chr1:169558381
|
C | T | 6 | a0018c0033t0006g0008a0018c0033t0006g0011a0019c0034t0002g0006others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+772G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558381 | ||||||
chr1:169558391
|
C | A | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.730+762G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558391 | ||||||
chr1:169558618
|
T | C | 143 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(140): Show | 144 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.730+535A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558618 | ||||||
chr1:169558707
|
C | T | 224 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(221): Show | 225 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.730+446G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558707 | ||||||
chr1:169558837
|
C | G | 143 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(140): Show | 144 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.730+316G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558837 | ||||||
chr1:169558859
|
C | T | 2 | a0001c0004t0002g0249a0003c0026t0004g0222 | 2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.730+294G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558859 | ||||||
chr1:169558942
|
C | A | 17 | a0002c0019t0001g0284a0004c0040t0002g0301a0004c0040t0003g0289others(14): Show | 17 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.730+211G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558942 | ||||||
chr1:169558945
|
T | A | 2 | a0005c0011t0001g0269a0005c0011t0001g0296 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.730+208A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169558945 | ||||||
chr1:169559005
|
T | TAAA | 84 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(81): Show | 84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.730+145_730+147dup others(3): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169559005 | ||||||
chr1:169559005
|
T | TAAAA | 56 | a0002c0019t0001g0053a0002c0019t0001g0284a0002c0070t0001g0277others(53): Show | 57 | HG00099.hp1 HG00738.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.730+144_730+147dup others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169559005 | ||||||
chr1:169559146
|
G | A | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.730+7C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 5/24 | chr1 | 169559146 | ||||||
chr1:169559342
|
C | T | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-46G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559342 | ||||||
chr1:169559426
|
T | A | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.587-130A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559426 | ||||||
chr1:169559484
|
C | T | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-188G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559484 | ||||||
chr1:169559592
|
C | T | 237 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(234): Show | 238 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.587-296G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559592 | ||||||
chr1:169559621
|
C | T | 3 | a0013c0039t0001g0127a0013c0039t0001g0139a0015c0038t0005g0112 | 3 | NA18993.hp1 NA18999.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.587-325G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559621 | ||||||
chr1:169559637
|
A | G | 1 | a0011c0036t0003g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.587-341T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559637 | ||||||
chr1:169559793
|
A | C | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-497T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559793 | ||||||
chr1:169559894
|
C | T | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-598G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559894 | ||||||
chr1:169559897
|
G | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-601C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559897 | ||||||
chr1:169559898
|
AGC | A | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-604_587-603del others(2): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559898 | ||||||
chr1:169559900
|
C | T | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.587-604G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559900 | ||||||
chr1:169559905
|
A | G | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-609T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559905 | ||||||
chr1:169559910
|
T | C | 1 | a0002c0019t0001g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.587-614A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559910 | ||||||
chr1:169559959
|
T | C | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+595A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169559959 | ||||||
chr1:169560234
|
A | G | 12 | a0009c0016t0003g0043a0009c0016t0003g0056a0009c0016t0003g0065others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.586+320T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169560234 | ||||||
chr1:169560408
|
T | G | 3 | a0009c0016t0003g0071a0009c0030t0006g0074a0041c0045t0005g0075 | 3 | HG01346.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.586+146A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169560408 | ||||||
chr1:169560517
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+37T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 4/24 | chr1 | 169560517 | ||||||
chr1:169560783
|
C | T | 1 | a0005c0006t0001g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.374-17G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169560783 | ||||||
chr1:169560832
|
A | C | 131 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(128): Show | 132 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.374-66T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169560832 | ||||||
chr1:169560839
|
G | T | 37 | a0009c0016t0003g0043a0009c0016t0003g0051a0009c0016t0003g0056others(34): Show | 38 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.374-73C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169560839 | ||||||
chr1:169560855
|
T | C | 131 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(128): Show | 132 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.374-89A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169560855 | ||||||
chr1:169560938
|
C | G | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.374-172G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169560938 | ||||||
chr1:169561070
|
T | C | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.374-304A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561070 | ||||||
chr1:169561082
|
C | T | 1 | a0002c0003t0004g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.374-316G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561082 | ||||||
chr1:169561123
|
G | C | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.374-357C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561123 | ||||||
chr1:169561143
|
C | T | 1 | a0003c0026t0004g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.374-377G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561143 | ||||||
chr1:169561288
|
T | TC | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-523dupG | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561288 | ||||||
chr1:169561293
|
C | CA | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.374-528_374-527ins others(1): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561293 | ||||||
chr1:169561325
|
T | C | 1 | a0001c0004t0002g0239 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.374-559A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561325 | ||||||
chr1:169561348
|
T | C | 143 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(140): Show | 144 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.374-582A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561348 | ||||||
chr1:169561528
|
G | A | 7 | a0002c0003t0004g0275a0004c0067t0002g0276a0007c0027t0002g0273others(4): Show | 7 | HG01081.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.374-762C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561528 | ||||||
chr1:169561564
|
G | A | 1 | a0014c0031t0001g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.374-798C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561564 | ||||||
chr1:169561599
|
G | T | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-833C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561599 | ||||||
chr1:169561743
|
C | A | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-977G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561743 | ||||||
chr1:169561785
|
C | G | 1 | a0004c0067t0002g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.374-1019G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561785 | ||||||
chr1:169561797
|
G | A | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-1031C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561797 | ||||||
chr1:169561847
|
C | A | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-1081G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561847 | ||||||
chr1:169561897
|
T | C | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-1131A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169561897 | ||||||
chr1:169562078
|
A | G | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.374-1312T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562078 | ||||||
chr1:169562166
|
C | T | 3 | a0013c0039t0001g0127a0013c0039t0001g0139a0015c0038t0005g0112 | 3 | NA18993.hp1 NA18999.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.374-1400G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562166 | ||||||
chr1:169562204
|
T | C | 242 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(239): Show | 243 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.374-1438A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562204 | ||||||
chr1:169562260
|
T | G | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.374-1494A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562260 | ||||||
chr1:169562333
|
T | C | 130 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.374-1567A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562333 | ||||||
chr1:169562411
|
CT | C | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-1646delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562411 | ||||||
chr1:169562522
|
A | G | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.374-1756T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562522 | ||||||
chr1:169562557
|
C | G | 1 | a0005c0006t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.374-1791G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562557 | ||||||
chr1:169562791
|
T | C | 1 | a0005c0008t0001g0209 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.374-2025A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562791 | ||||||
chr1:169562868
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.374-2102A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562868 | ||||||
chr1:169562873
|
C | T | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-2107G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562873 | ||||||
chr1:169562921
|
C | T | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-2155G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169562921 | ||||||
chr1:169563100
|
C | A | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.374-2334G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563100 | ||||||
chr1:169563389
|
A | C | 1 | a0007c0013t0002g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.374-2623T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563389 | ||||||
chr1:169563395
|
T | C | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-2629A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563395 | ||||||
chr1:169563445
|
A | G | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.374-2679T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563445 | ||||||
chr1:169563629
|
A | G | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-2863T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563629 | ||||||
chr1:169563657
|
T | A | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-2891A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563657 | ||||||
chr1:169563774
|
C | T | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.374-3008G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563774 | ||||||
chr1:169563833
|
C | T | 2 | a0021c0057t0002g0298a0022c0058t0003g0299 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.374-3067G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563833 | ||||||
chr1:169563855
|
CTCTT | C | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-3093_374-3090d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563855 | ||||||
chr1:169563924
|
T | G | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.374-3158A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563924 | ||||||
chr1:169563949
|
A | C | 3 | a0002c0003t0001g0013a0002c0003t0001g0015a0007c0041t0006g0014 | 3 | HG03486.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.374-3183T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563949 | ||||||
chr1:169563986
|
A | G | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-3220T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169563986 | ||||||
chr1:169564028
|
G | A | 224 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(221): Show | 225 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.374-3262C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564028 | ||||||
chr1:169564108
|
A | T | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-3342T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564108 | ||||||
chr1:169564164
|
A | C | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-3398T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564164 | ||||||
chr1:169564379
|
C | T | 1 | a0003c0032t0004g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.374-3613G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564379 | ||||||
chr1:169564472
|
C | T | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.374-3706G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564472 | ||||||
chr1:169564506
|
T | A | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.374-3740A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564506 | ||||||
chr1:169564607
|
G | T | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-3841C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564607 | ||||||
chr1:169564639
|
T | C | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.374-3873A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564639 | ||||||
chr1:169564790
|
T | C | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.374-4024A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564790 | ||||||
chr1:169564816
|
C | A | 1 | a0007c0013t0002g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.374-4050G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564816 | ||||||
chr1:169564911
|
T | C | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-4145A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169564911 | ||||||
chr1:169565276
|
G | A | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-4510C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565276 | ||||||
chr1:169565346
|
A | G | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.374-4580T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565346 | ||||||
chr1:169565433
|
A | C | 9 | a0002c0019t0001g0053a0003c0018t0003g0026a0003c0018t0003g0048others(6): Show | 9 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.374-4667T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565433 | ||||||
chr1:169565501
|
G | T | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.374-4735C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565501 | ||||||
chr1:169565515
|
G | T | 1 | a0002c0003t0001g0025 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.374-4749C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565515 | ||||||
chr1:169565581
|
C | T | 11 | a0004c0040t0002g0301a0004c0059t0001g0300a0018c0033t0006g0008others(8): Show | 11 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.374-4815G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565581 | ||||||
chr1:169565607
|
T | C | 2 | a0019c0034t0002g0006a0043c0044t0001g0007 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.374-4841A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565607 | ||||||
chr1:169565650
|
A | G | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-4884T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565650 | ||||||
chr1:169565692
|
A | G | 1 | a0031c0053t0001g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.374-4926T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565692 | ||||||
chr1:169565728
|
T | A | 127 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(124): Show | 128 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.374-4962A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565728 | ||||||
chr1:169565728
|
T | C | 117 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(114): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.374-4962A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565728 | ||||||
chr1:169565800
|
G | A | 2 | a0002c0070t0001g0277a0005c0011t0001g0020 | 2 | HG02723.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.374-5034C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565800 | ||||||
chr1:169565819
|
T | C | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.374-5053A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565819 | ||||||
chr1:169565830
|
C | T | 1 | a0004c0021t0006g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.374-5064G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565830 | ||||||
chr1:169565880
|
C | T | 1 | a0001c0004t0002g0226 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.374-5114G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565880 | ||||||
chr1:169565958
|
T | G | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-5192A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565958 | ||||||
chr1:169565986
|
A | T | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.374-5220T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169565986 | ||||||
chr1:169566012
|
T | C | 1 | a0002c0003t0004g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.374-5246A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566012 | ||||||
chr1:169566115
|
C | G | 224 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(221): Show | 225 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.374-5349G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566115 | ||||||
chr1:169566141
|
T | A | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.374-5375A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566141 | ||||||
chr1:169566205
|
A | G | 1 | a0004c0007t0003g0264 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.374-5439T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566205 | ||||||
chr1:169566337
|
G | T | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.374-5571C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566337 | ||||||
chr1:169566395
|
A | C | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.374-5629T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566395 | ||||||
chr1:169566420
|
T | G | 1 | a0001c0004t0002g0228 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.374-5654A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566420 | ||||||
chr1:169566514
|
T | G | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+5707A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566514 | ||||||
chr1:169566531
|
G | A | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+5690C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566531 | ||||||
chr1:169566587
|
G | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.373+5634C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566587 | ||||||
chr1:169566600
|
A | G | 3 | a0002c0003t0001g0220a0004c0021t0001g0221a0007c0063t0006g0261 | 3 | HG02055.hp1 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.373+5621T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566600 | ||||||
chr1:169566612
|
GA | G | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+5608delT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566612 | ||||||
chr1:169566680
|
A | G | 69 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(66): Show | 69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.373+5541T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566680 | ||||||
chr1:169566774
|
T | G | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.373+5447A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566774 | ||||||
chr1:169566827
|
G | A | 3 | a0004c0023t0003g0155a0004c0023t0003g0186a0004c0023t0003g0198 | 3 | HG01069.hp1 HG01071.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.373+5394C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566827 | ||||||
chr1:169566929
|
T | C | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.373+5292A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169566929 | ||||||
chr1:169567002
|
C | A | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+5219G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567002 | ||||||
chr1:169567100
|
G | A | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+5121C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567100 | ||||||
chr1:169567201
|
C | T | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.373+5020G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567201 | ||||||
chr1:169567247
|
G | A | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.373+4974C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567247 | ||||||
chr1:169567247
|
G | C | 94 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+4974C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567247 | ||||||
chr1:169567264
|
G | T | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.373+4957C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567264 | ||||||
chr1:169567383
|
T | TA | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.373+4837dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567383 | ||||||
chr1:169567383
|
T | TAAAA | 12 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(9): Show | 12 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.373+4834_373+4837d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567383 | ||||||
chr1:169567412
|
G | A | 224 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(221): Show | 225 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.373+4809C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567412 | ||||||
chr1:169567542
|
CT | C | 145 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(142): Show | 146 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.373+4678delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567542 | ||||||
chr1:169567542
|
CTT | C | 83 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(80): Show | 83 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.373+4677_373+4678d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567542 | ||||||
chr1:169567663
|
G | A | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.373+4558C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567663 | ||||||
chr1:169567676
|
A | T | 1 | a0001c0004t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.373+4545T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567676 | ||||||
chr1:169567772
|
C | A | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.373+4449G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567772 | ||||||
chr1:169567798
|
G | A | 5 | a0009c0030t0001g0038a0010c0012t0002g0037a0014c0031t0001g0035others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.373+4423C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169567798 | ||||||
chr1:169568023
|
C | T | 5 | a0010c0012t0002g0061a0010c0012t0002g0062a0010c0012t0002g0063others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.373+4198G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568023 | ||||||
chr1:169568049
|
G | T | 2 | a0002c0003t0001g0253a0002c0003t0001g0254 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.373+4172C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568049 | ||||||
chr1:169568064
|
G | A | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.373+4157C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568064 | ||||||
chr1:169568105
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.373+4116T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568105 | ||||||
chr1:169568131
|
G | A | 2 | a0021c0057t0002g0298a0022c0058t0003g0299 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.373+4090C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568131 | ||||||
chr1:169568342
|
C | A | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.373+3879G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568342 | ||||||
chr1:169568349
|
G | A | 1 | a0002c0003t0001g0248 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.373+3872C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568349 | ||||||
chr1:169568440
|
A | G | 237 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(234): Show | 238 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.373+3781T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568440 | ||||||
chr1:169568476
|
G | A | 2 | a0004c0021t0006g0295a0028c0065t0003g0260 | 2 | HG00735.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.373+3745C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568476 | ||||||
chr1:169568528
|
CT | C | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+3692delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568528 | ||||||
chr1:169568581
|
G | A | 1 | a0003c0005t0003g0034 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.373+3640C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568581 | ||||||
chr1:169568701
|
C | T | 2 | a0005c0008t0001g0165a0005c0008t0001g0171 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.373+3520G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568701 | ||||||
chr1:169568725
|
T | C | 1 | a0001c0074t0002g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.373+3496A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568725 | ||||||
chr1:169568893
|
T | C | 1 | a0004c0007t0003g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.373+3328A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568893 | ||||||
chr1:169568936
|
G | C | 1 | a0004c0021t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.373+3285C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169568936 | ||||||
chr1:169569009
|
C | T | 98 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.373+3212G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569009 | ||||||
chr1:169569107
|
G | A | 50 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(47): Show | 50 | HG00423.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.373+3114C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569107 | ||||||
chr1:169569159
|
G | A | 1 | a0003c0005t0003g0029 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.373+3062C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569159 | ||||||
chr1:169569188
|
A | G | 5 | a0004c0040t0002g0301a0004c0059t0001g0300a0021c0057t0002g0298others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.373+3033T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569188 | ||||||
chr1:169569228
|
G | A | 47 | a0002c0019t0001g0053a0003c0018t0003g0026a0003c0018t0003g0048others(44): Show | 48 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.373+2993C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569228 | ||||||
chr1:169569306
|
C | T | 124 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.373+2915G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569306 | ||||||
chr1:169569339
|
A | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.373+2882T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569339 | ||||||
chr1:169569358
|
C | G | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+2863G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569358 | ||||||
chr1:169569365
|
T | G | 129 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(126): Show | 130 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.373+2856A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569365 | ||||||
chr1:169569604
|
C | T | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+2617G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569604 | ||||||
chr1:169569895
|
A | C | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.373+2326T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169569895 | ||||||
chr1:169570045
|
G | A | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+2176C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570045 | ||||||
chr1:169570110
|
T | G | 37 | a0009c0016t0003g0043a0009c0016t0003g0051a0009c0016t0003g0056others(34): Show | 38 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.373+2111A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570110 | ||||||
chr1:169570408
|
C | T | 3 | a0003c0022t0004g0016a0007c0041t0006g0014a0007c0041t0008g0017 | 3 | HG02922.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.373+1813G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570408 | ||||||
chr1:169570412
|
T | C | 1 | a0007c0041t0008g0017 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.373+1809A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570412 | ||||||
chr1:169570473
|
T | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.373+1748A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570473 | ||||||
chr1:169570569
|
C | T | 1 | a0003c0026t0003g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.373+1652G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570569 | ||||||
chr1:169570583
|
T | G | 1 | a0011c0017t0004g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.373+1638A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570583 | ||||||
chr1:169570685
|
C | T | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+1536G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570685 | ||||||
chr1:169570710
|
A | AT | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.373+1510dupA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570710 | ||||||
chr1:169570842
|
C | T | 101 | a0001c0001t0002g0090a0001c0001t0002g0100a0001c0001t0002g0101others(98): Show | 101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.373+1379G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169570842 | ||||||
chr1:169571038
|
T | TAGG | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+1182_373+1183i others(5): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571038 | ||||||
chr1:169571053
|
TTAAA | T | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+1164_373+1167d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571053 | ||||||
chr1:169571096
|
C | A | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.373+1125G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571096 | ||||||
chr1:169571184
|
A | G | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.373+1037T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571184 | ||||||
chr1:169571305
|
A | G | 1 | a0001c0004t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.373+916T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571305 | ||||||
chr1:169571315
|
C | T | 5 | a0004c0040t0002g0301a0004c0059t0001g0300a0021c0057t0002g0298others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.373+906G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571315 | ||||||
chr1:169571354
|
T | C | 106 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(103): Show | 106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.373+867A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571354 | ||||||
chr1:169571490
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.373+731T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571490 | ||||||
chr1:169571574
|
T | C | 1 | a0004c0021t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.373+647A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571574 | ||||||
chr1:169571658
|
A | C | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.373+563T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571658 | ||||||
chr1:169571696
|
C | T | 6 | a0018c0033t0006g0008a0018c0033t0006g0011a0019c0034t0002g0006others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.373+525G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571696 | ||||||
chr1:169571733
|
C | T | 4 | a0003c0015t0004g0123a0003c0015t0004g0124a0005c0006t0001g0122others(1): Show | 4 | HG01123.hp1 HG01361.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+488G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571733 | ||||||
chr1:169571757
|
G | A | 7 | a0002c0003t0004g0275a0004c0067t0002g0276a0007c0027t0002g0273others(4): Show | 7 | HG01081.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+464C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571757 | ||||||
chr1:169571767
|
C | A | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.373+454G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571767 | ||||||
chr1:169571862
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.373+359T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571862 | ||||||
chr1:169571927
|
T | C | 6 | a0002c0003t0001g0013a0002c0003t0001g0015a0003c0022t0004g0016others(3): Show | 6 | HG02886.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.373+294A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571927 | ||||||
chr1:169571960
|
A | G | 1 | a0001c0004t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.373+261T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169571960 | ||||||
chr1:169572128
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.373+93T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169572128 | ||||||
chr1:169572133
|
G | A | 4 | a0009c0016t0003g0043a0012c0024t0007g0047a0012c0024t0007g0072others(1): Show | 4 | HG01884.hp2 HG03041.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+88C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 3/24 | chr1 | 169572133 | ||||||
chr1:169572382
|
G | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-39C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572382 | ||||||
chr1:169572406
|
C | T | 1 | a0002c0019t0018g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.251-63G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572406 | ||||||
chr1:169572521
|
A | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-178T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572521 | ||||||
chr1:169572565
|
C | G | 1 | a0004c0023t0003g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.251-222G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572565 | ||||||
chr1:169572602
|
G | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-259C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572602 | ||||||
chr1:169572688
|
G | T | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251-345C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572688 | ||||||
chr1:169572724
|
C | A | 5 | a0003c0073t0004g0039a0004c0069t0001g0288a0005c0071t0001g0293others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-381G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572724 | ||||||
chr1:169572778
|
T | A | 1 | a0001c0004t0002g0024 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.251-435A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572778 | ||||||
chr1:169572897
|
C | T | 100 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.251-554G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572897 | ||||||
chr1:169572949
|
TTTC | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-609_251-607del others(3): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572949 | ||||||
chr1:169572952
|
C | CT | 14 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(11): Show | 14 | HG01168.hp1 HG02155.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.251-610dupA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572952 | ||||||
chr1:169572952
|
CTTT | C | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-612_251-610del others(3): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572952 | ||||||
chr1:169572968
|
T | C | 1 | a0009c0030t0006g0074 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.251-625A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572968 | ||||||
chr1:169572977
|
G | A | 2 | a0019c0034t0002g0006a0043c0044t0001g0007 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.251-634C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169572977 | ||||||
chr1:169573024
|
T | C | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-681A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573024 | ||||||
chr1:169573178
|
C | T | 1 | a0004c0007t0003g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.251-835G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573178 | ||||||
chr1:169573197
|
C | G | 1 | a0001c0001t0002g0094 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.251-854G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573197 | ||||||
chr1:169573228
|
G | T | 1 | a0001c0001t0002g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.251-885C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573228 | ||||||
chr1:169573233
|
CCACCA | C | 4 | a0002c0019t0001g0284a0007c0013t0002g0278a0007c0013t0002g0282others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-895_251-891del others(5): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573233 | ||||||
chr1:169573244
|
C | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-901G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573244 | ||||||
chr1:169573368
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-1025T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573368 | ||||||
chr1:169573404
|
A | T | 1 | a0001c0001t0002g0110 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.251-1061T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573404 | ||||||
chr1:169573405
|
T | C | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-1062A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573405 | ||||||
chr1:169573443
|
A | G | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.251-1100T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573443 | ||||||
chr1:169573459
|
C | T | 1 | a0026c0051t0002g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251-1116G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573459 | ||||||
chr1:169573462
|
G | A | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-1119C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573462 | ||||||
chr1:169573474
|
T | C | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.251-1131A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573474 | ||||||
chr1:169573479
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.251-1136C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573479 | ||||||
chr1:169573479
|
G | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-1136C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573479 | ||||||
chr1:169573503
|
C | T | 1 | a0009c0016t0003g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.251-1160G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573503 | ||||||
chr1:169573512
|
C | A | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.251-1169G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573512 | ||||||
chr1:169573531
|
T | C | 3 | a0005c0006t0001g0280a0007c0013t0006g0283a0029c0052t0002g0281 | 3 | HG01884.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.251-1188A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573531 | ||||||
chr1:169573561
|
C | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-1218G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573561 | ||||||
chr1:169573654
|
A | C | 2 | a0019c0034t0002g0006a0043c0044t0001g0007 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.251-1311T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573654 | ||||||
chr1:169573711
|
C | A | 1 | a0004c0023t0003g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.251-1368G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573711 | ||||||
chr1:169573784
|
C | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-1441G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573784 | ||||||
chr1:169573785
|
G | A | 5 | a0003c0073t0004g0039a0004c0069t0001g0288a0005c0071t0001g0293others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1442C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573785 | ||||||
chr1:169573794
|
G | A | 1 | a0003c0026t0003g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.251-1451C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573794 | ||||||
chr1:169573812
|
CAGA | C | 5 | a0004c0040t0002g0301a0004c0059t0001g0300a0021c0057t0002g0298others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1472_251-1470d others(5): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573812 | ||||||
chr1:169573893
|
G | A | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.251-1550C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169573893 | ||||||
chr1:169574025
|
C | A | 244 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(241): Show | 245 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.251-1682G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574025 | ||||||
chr1:169574066
|
G | A | 3 | a0006c0009t0005g0055a0006c0009t0005g0078a0006c0009t0005g0079 | 3 | HG01069.hp2 HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.251-1723C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574066 | ||||||
chr1:169574253
|
TGGAGTCT others(1): Show |
T | 5 | a0004c0007t0003g0264a0004c0007t0003g0266a0004c0007t0003g0267others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1918_251-1911d others(10): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574253 | ||||||
chr1:169574434
|
A | C | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.251-2091T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574434 | ||||||
chr1:169574512
|
G | A | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-2169C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574512 | ||||||
chr1:169574539
|
G | A | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-2196C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574539 | ||||||
chr1:169574805
|
T | A | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-2462A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574805 | ||||||
chr1:169574912
|
T | C | 1 | a0013c0039t0001g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.251-2569A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574912 | ||||||
chr1:169574985
|
A | G | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251-2642T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574985 | ||||||
chr1:169574996
|
C | A | 100 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.251-2653G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169574996 | ||||||
chr1:169575055
|
A | G | 1 | a0031c0053t0001g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.251-2712T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575055 | ||||||
chr1:169575149
|
C | T | 113 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.251-2806G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575149 | ||||||
chr1:169575234
|
C | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-2891G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575234 | ||||||
chr1:169575414
|
A | G | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.251-3071T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575414 | ||||||
chr1:169575463
|
A | C | 1 | a0004c0050t0003g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.251-3120T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575463 | ||||||
chr1:169575509
|
C | T | 1 | a0004c0007t0003g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.251-3166G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575509 | ||||||
chr1:169575510
|
G | A | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251-3167C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575510 | ||||||
chr1:169575552
|
A | G | 1 | a0004c0023t0003g0198 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.251-3209T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575552 | ||||||
chr1:169575714
|
A | G | 100 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.251-3371T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575714 | ||||||
chr1:169575809
|
C | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-3466G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575809 | ||||||
chr1:169575827
|
C | T | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-3484G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575827 | ||||||
chr1:169575828
|
G | A | 5 | a0004c0069t0001g0288a0005c0006t0001g0280a0007c0013t0006g0283others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-3485C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575828 | ||||||
chr1:169575883
|
T | C | 1 | a0004c0025t0001g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.251-3540A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575883 | ||||||
chr1:169575890
|
G | T | 95 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.251-3547C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169575890 | ||||||
chr1:169576040
|
C | T | 3 | a0007c0013t0002g0278a0007c0013t0002g0282a0007c0013t0002g0285 | 3 | HG02647.hp2 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.251-3697G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576040 | ||||||
chr1:169576174
|
C | G | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-3831G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576174 | ||||||
chr1:169576175
|
A | G | 238 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(235): Show | 239 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.251-3832T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576175 | ||||||
chr1:169576184
|
T | A | 106 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(103): Show | 106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.251-3841A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576184 | ||||||
chr1:169576214
|
G | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-3871C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576214 | ||||||
chr1:169576316
|
C | T | 1 | a0003c0032t0004g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.251-3973G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576316 | ||||||
chr1:169576327
|
T | C | 2 | a0002c0003t0001g0220a0004c0021t0001g0221 | 2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.251-3984A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576327 | ||||||
chr1:169576349
|
C | G | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-4006G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576349 | ||||||
chr1:169576454
|
A | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-4111T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576454 | ||||||
chr1:169576471
|
A | C | 1 | a0004c0069t0001g0288 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.251-4128T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576471 | ||||||
chr1:169576584
|
G | A | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-4241C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576584 | ||||||
chr1:169576597
|
G | A | 82 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.251-4254C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576597 | ||||||
chr1:169576710
|
A | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-4367T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169576710 | ||||||
chr1:169577015
|
C | T | 11 | a0004c0040t0002g0301a0004c0059t0001g0300a0018c0033t0006g0008others(8): Show | 11 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.251-4672G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577015 | ||||||
chr1:169577016
|
G | A | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251-4673C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577016 | ||||||
chr1:169577089
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-4746T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577089 | ||||||
chr1:169577090
|
C | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-4747G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577090 | ||||||
chr1:169577171
|
G | A | 2 | a0004c0040t0002g0301a0004c0059t0001g0300 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.251-4828C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577171 | ||||||
chr1:169577259
|
A | T | 2 | a0002c0003t0004g0275a0024c0066t0003g0270 | 2 | HG01081.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.251-4916T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577259 | ||||||
chr1:169577519
|
G | A | 2 | a0002c0003t0001g0005a0002c0003t0001g0262 | 3 | HG01123.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.250+4912C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577519 | ||||||
chr1:169577547
|
T | C | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+4884A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577547 | ||||||
chr1:169577557
|
T | TTATATAT others(7): Show |
1 | a0004c0023t0003g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.250+4873_250+4874i others(16): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577557 | ||||||
chr1:169577560
|
A | AAT | 9 | a0001c0004t0002g0239a0002c0003t0001g0005a0002c0003t0001g0220others(6): Show | 10 | HG01123.hp2 HG01175.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+4869_250+4870d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATAT | 11 | a0001c0002t0002g0205a0003c0005t0003g0032a0003c0022t0019g0235others(8): Show | 11 | HG00423.hp1 HG01981.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+4867_250+4870d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATAT | 8 | a0001c0002t0002g0199a0001c0002t0002g0200a0002c0010t0001g0201others(5): Show | 8 | HG00280.hp1 HG02559.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+4865_250+4870d others(8): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(1): Show |
14 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0196others(11): Show | 14 | HG00408.hp1 HG01168.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+4863_250+4870d others(10): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(3): Show |
14 | a0001c0002t0002g0030a0001c0002t0002g0188a0001c0002t0002g0189others(11): Show | 14 | HG01071.hp1 HG01256.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+4861_250+4870d others(12): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(5): Show |
4 | a0002c0010t0001g0181a0002c0029t0001g0182a0003c0005t0003g0029others(1): Show | 4 | HG01258.hp2 NA18522.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+4859_250+4870d others(14): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(7): Show |
12 | a0001c0002t0002g0176a0001c0002t0002g0178a0001c0004t0010g0231others(9): Show | 12 | HG01261.hp2 HG01346.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+4857_250+4870d others(16): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(9): Show |
7 | a0001c0002t0002g0028a0001c0002t0002g0173a0001c0002t0002g0174others(4): Show | 7 | HG00639.hp2 HG01934.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+4855_250+4870d others(18): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(11): Show |
8 | a0001c0002t0002g0169a0001c0004t0002g0230a0005c0008t0001g0165others(5): Show | 8 | HG00735.hp1 HG01081.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+4853_250+4870d others(20): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(13): Show |
11 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0162others(8): Show | 11 | HG00280.hp2 HG01884.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.250+4851_250+4870d others(22): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(15): Show |
3 | a0001c0002t0002g0157a0001c0002t0002g0158a0003c0005t0003g0156 | 3 | HG01496.hp2 HG04115.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.250+4849_250+4870d others(24): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(17): Show |
3 | a0003c0022t0004g0229a0004c0023t0003g0155a0006c0028t0005g0154 | 3 | HG01069.hp1 NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.250+4847_250+4870d others(26): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | AATATATA others(19): Show |
1 | a0003c0005t0003g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.250+4845_250+4870d others(28): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | ATATATAT others(6): Show |
1 | a0003c0005t0003g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.250+4870_250+4871i others(15): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | ATATATAT others(8): Show |
1 | a0002c0010t0001g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.250+4870_250+4871i others(17): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | ATATATAT others(12): Show |
1 | a0003c0005t0003g0033 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.250+4870_250+4871i others(21): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | ATATATAT others(14): Show |
1 | a0003c0005t0003g0027 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.250+4870_250+4871i others(23): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
A | T | 2 | a0003c0005t0004g0151a0004c0023t0003g0152 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.250+4871T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AAT | A | 17 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0004t0010g0247others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.250+4869_250+4870d others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATAT | A | 14 | a0001c0001t0002g0094a0001c0001t0002g0098a0001c0004t0002g0249others(11): Show | 14 | HG01169.hp1 HG01515.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+4867_250+4870d others(6): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATAT | A | 27 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(24): Show | 28 | HG00673.hp2 HG00733.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.250+4865_250+4870d others(8): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(1): Show |
A | 29 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0113others(26): Show | 30 | HG00099.hp1 HG00423.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.250+4863_250+4870d others(10): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(3): Show |
A | 40 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0133others(37): Show | 41 | HG00408.hp2 HG00639.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.250+4861_250+4870d others(12): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(5): Show |
A | 12 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0140others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+4859_250+4870d others(14): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(7): Show |
A | 1 | a0004c0050t0003g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.250+4857_250+4870d others(16): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(15): Show |
A | 1 | a0033c0080t0017g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+4849_250+4870d others(24): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(17): Show |
A | 2 | a0002c0010t0001g0210a0006c0028t0005g0219 | 2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.250+4847_250+4870d others(26): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577560
|
AATATATA others(25): Show |
A | 1 | a0007c0063t0006g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250+4839_250+4870d others(34): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577560 | ||||||
chr1:169577577
|
ATATATAT others(21): Show |
A | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+4826_250+4853d others(30): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577577 | ||||||
chr1:169577579
|
ATATATAT others(19): Show |
A | 17 | a0003c0073t0004g0039a0004c0040t0002g0301a0004c0040t0003g0289others(14): Show | 17 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.250+4826_250+4851d others(28): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577579 | ||||||
chr1:169577581
|
ATATATAT others(17): Show |
A | 3 | a0001c0004t0002g0023a0001c0004t0002g0024a0032c0060t0005g0297 | 3 | HG02155.hp2 NA18522.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.250+4826_250+4849d others(26): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577581 | ||||||
chr1:169577601
|
A | G | 1 | a0004c0050t0003g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.250+4830T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577601 | ||||||
chr1:169577605
|
G | A | 8 | a0002c0003t0001g0013a0002c0003t0001g0019a0002c0003t0001g0025others(5): Show | 9 | HG01168.hp1 HG02132.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+4826C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577605 | ||||||
chr1:169577628
|
C | T | 2 | a0002c0010t0001g0149a0002c0010t0001g0150 | 2 | NA18973.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.250+4803G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577628 | ||||||
chr1:169577695
|
C | A | 1 | a0001c0002t0002g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250+4736G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577695 | ||||||
chr1:169577696
|
T | C | 12 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(9): Show | 12 | HG01168.hp1 HG02109.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.250+4735A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577696 | ||||||
chr1:169577748
|
C | G | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+4683G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577748 | ||||||
chr1:169577929
|
C | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+4502G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169577929 | ||||||
chr1:169578029
|
G | A | 1 | a0002c0003t0001g0025 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.250+4402C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578029 | ||||||
chr1:169578095
|
C | T | 2 | a0006c0009t0005g0081a0006c0009t0005g0082 | 2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.250+4336G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578095 | ||||||
chr1:169578131
|
T | A | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+4300A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578131 | ||||||
chr1:169578169
|
A | C | 25 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(22): Show | 25 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.250+4262T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578169 | ||||||
chr1:169578171
|
T | C | 3 | a0003c0073t0004g0039a0005c0071t0001g0293a0034c0072t0005g0292 | 3 | HG02258.hp1 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.250+4260A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578171 | ||||||
chr1:169578220
|
G | T | 1 | a0005c0006t0001g0080 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.250+4211C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578220 | ||||||
chr1:169578222
|
C | T | 1 | a0004c0007t0003g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.250+4209G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578222 | ||||||
chr1:169578239
|
C | T | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+4192G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578239 | ||||||
chr1:169578347
|
A | G | 1 | a0004c0023t0003g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250+4084T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578347 | ||||||
chr1:169578372
|
A | C | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+4059T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578372 | ||||||
chr1:169578479
|
G | A | 8 | a0002c0003t0001g0005a0002c0003t0001g0262a0002c0070t0001g0277others(5): Show | 9 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+3952C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578479 | ||||||
chr1:169578519
|
G | C | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.250+3912C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578519 | ||||||
chr1:169578562
|
C | T | 1 | a0004c0023t0003g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250+3869G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578562 | ||||||
chr1:169578581
|
A | T | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+3850T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578581 | ||||||
chr1:169578637
|
C | G | 1 | a0032c0060t0005g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250+3794G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578637 | ||||||
chr1:169578774
|
A | G | 3 | a0001c0004t0002g0226a0001c0004t0002g0227a0001c0004t0002g0228 | 3 | NA18951.hp1 NA18985.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.250+3657T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578774 | ||||||
chr1:169578815
|
A | G | 10 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(7): Show | 10 | HG01168.hp1 HG02155.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.250+3616T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578815 | ||||||
chr1:169578836
|
C | A | 2 | a0004c0040t0003g0289a0007c0056t0008g0290 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.250+3595G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578836 | ||||||
chr1:169578968
|
G | C | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+3463C>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169578968 | ||||||
chr1:169579053
|
C | T | 2 | a0005c0011t0009g0001a0006c0020t0005g0225 | 3 | HG00738.hp1 HG01515.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.250+3378G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579053 | ||||||
chr1:169579063
|
C | T | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+3368G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579063 | ||||||
chr1:169579211
|
A | G | 15 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(12): Show | 15 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.250+3220T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579211 | ||||||
chr1:169579277
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.250+3154G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579277 | ||||||
chr1:169579608
|
C | T | 1 | a0007c0013t0002g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.250+2823G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579608 | ||||||
chr1:169579632
|
C | A | 1 | a0011c0036t0003g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250+2799G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579632 | ||||||
chr1:169579654
|
C | A | 111 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(108): Show | 111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.250+2777G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579654 | ||||||
chr1:169579662
|
A | T | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+2769T>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579662 | ||||||
chr1:169579802
|
T | C | 20 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(17): Show | 20 | HG01168.hp1 HG02109.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.250+2629A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579802 | ||||||
chr1:169579840
|
T | C | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+2591A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579840 | ||||||
chr1:169579855
|
C | A | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.250+2576G>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169579855 | ||||||
chr1:169580125
|
A | G | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+2306T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580125 | ||||||
chr1:169580364
|
T | C | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+2067A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580364 | ||||||
chr1:169580387
|
TG | T | 8 | a0004c0040t0003g0289a0007c0056t0008g0290a0018c0033t0006g0008others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+2043delC | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580387 | ||||||
chr1:169580388
|
G | T | 2 | a0002c0003t0001g0224a0006c0020t0005g0223 | 2 | HG01243.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.250+2043C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580388 | ||||||
chr1:169580388
|
GT | G | 16 | a0001c0002t0002g0212a0001c0004t0002g0023a0001c0004t0002g0024others(13): Show | 16 | HG01168.hp1 HG02109.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.250+2042delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580388 | ||||||
chr1:169580391
|
T | G | 79 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.250+2040A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580391 | ||||||
chr1:169580392
|
T | G | 3 | a0002c0070t0001g0277a0004c0069t0001g0288a0027c0068t0004g0287 | 3 | HG02109.hp1 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.250+2039A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580392 | ||||||
chr1:169580394
|
T | G | 4 | a0001c0001t0002g0140a0001c0001t0002g0141a0002c0003t0001g0015others(1): Show | 4 | HG03579.hp1 NA18960.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+2037A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580394 | ||||||
chr1:169580395
|
T | G | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.250+2036A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580395 | ||||||
chr1:169580446
|
C | T | 3 | a0003c0073t0004g0039a0005c0071t0001g0293a0034c0072t0005g0292 | 3 | HG02258.hp1 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.250+1985G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580446 | ||||||
chr1:169580532
|
T | C | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+1899A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580532 | ||||||
chr1:169580537
|
T | C | 245 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(242): Show | 246 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.250+1894A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580537 | ||||||
chr1:169580571
|
G | A | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250+1860C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580571 | ||||||
chr1:169580573
|
G | T | 125 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(122): Show | 126 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.250+1858C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580573 | ||||||
chr1:169580939
|
C | T | 9 | a0002c0003t0001g0013a0002c0003t0001g0015a0003c0073t0004g0039others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+1492G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169580939 | ||||||
chr1:169581098
|
C | G | 29 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0013others(26): Show | 29 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.250+1333G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581098 | ||||||
chr1:169581182
|
G | GA | 7 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0019others(4): Show | 7 | HG01168.hp1 HG02155.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+1248dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581182 | ||||||
chr1:169581219
|
G | A | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.250+1212C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581219 | ||||||
chr1:169581300
|
T | C | 1 | a0002c0079t0001g0216 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.250+1131A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581300 | ||||||
chr1:169581352
|
G | T | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0013others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+1079C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581352 | ||||||
chr1:169581353
|
A | C | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.250+1078T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581353 | ||||||
chr1:169581446
|
AT | A | 14 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(11): Show | 14 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.250+984delA | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581446 | ||||||
chr1:169581509
|
G | A | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.250+922C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581509 | ||||||
chr1:169581511
|
C | T | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0013others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+920G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581511 | ||||||
chr1:169581525
|
T | G | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.250+906A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581525 | ||||||
chr1:169581725
|
G | A | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0013others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.250+706C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581725 | ||||||
chr1:169581835
|
TAAAC | T | 81 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0157others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.250+592_250+595del others(4): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581835 | ||||||
chr1:169581856
|
A | C | 6 | a0018c0033t0006g0008a0018c0033t0006g0011a0019c0034t0002g0006others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+575T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581856 | ||||||
chr1:169581883
|
T | C | 1 | a0002c0003t0001g0025 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.250+548A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581883 | ||||||
chr1:169581935
|
C | T | 1 | a0006c0028t0005g0147 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250+496G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169581935 | ||||||
chr1:169582196
|
G | A | 3 | a0001c0001t0002g0145a0002c0019t0001g0143a0008c0014t0001g0144 | 3 | NA18971.hp2 NA18975.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.250+235C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582196 | ||||||
chr1:169582202
|
G | A | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.250+229C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582202 | ||||||
chr1:169582297
|
T | C | 2 | a0003c0005t0003g0217a0003c0005t0003g0218 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.250+134A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582297 | ||||||
chr1:169582311
|
T | TA | 123 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(120): Show | 124 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.250+119dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582311 | ||||||
chr1:169582311
|
T | TAA | 20 | a0001c0001t0002g0146a0001c0004t0002g0023a0001c0004t0002g0024others(17): Show | 20 | HG02109.hp2 HG02155.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.250+118_250+119dup others(2): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582311 | ||||||
chr1:169582311
|
T | TAAA | 6 | a0002c0003t0001g0013a0002c0003t0001g0015a0002c0003t0001g0025others(3): Show | 6 | HG01168.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+117_250+119dup others(3): Show |
F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582311 | ||||||
chr1:169582327
|
C | T | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.250+104G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582327 | ||||||
chr1:169582390
|
A | C | 1 | a0003c0026t0004g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250+41T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 2/24 | chr1 | 169582390 | ||||||
chr1:169582554
|
G | A | 1 | a0006c0028t0005g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.159-32C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169582554 | ||||||
chr1:169582628
|
C | T | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-106G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169582628 | ||||||
chr1:169582730
|
A | G | 1 | a0007c0013t0002g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159-208T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169582730 | ||||||
chr1:169583007
|
G | T | 5 | a0009c0030t0001g0038a0010c0012t0002g0037a0014c0031t0001g0035others(2): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-485C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583007 | ||||||
chr1:169583045
|
T | C | 20 | a0002c0003t0001g0013a0002c0003t0001g0015a0002c0070t0001g0277others(17): Show | 20 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.159-523A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583045 | ||||||
chr1:169583424
|
G | A | 2 | a0004c0069t0001g0288a0027c0068t0004g0287 | 2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.159-902C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583424 | ||||||
chr1:169583527
|
C | T | 8 | a0001c0002t0002g0028a0001c0002t0002g0030a0003c0005t0003g0027others(5): Show | 8 | HG00423.hp1 HG02135.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.159-1005G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583527 | ||||||
chr1:169583545
|
G | A | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-1023C>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583545 | ||||||
chr1:169583779
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-1257T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583779 | ||||||
chr1:169583872
|
A | C | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-1350T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583872 | ||||||
chr1:169583962
|
A | C | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-1440T>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169583962 | ||||||
chr1:169584069
|
A | G | 1 | a0003c0018t0003g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159-1547T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584069 | ||||||
chr1:169584151
|
A | G | 1 | a0004c0021t0006g0295 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.159-1629T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584151 | ||||||
chr1:169584302
|
C | G | 26 | a0001c0004t0002g0023a0001c0004t0002g0024a0002c0003t0001g0013others(23): Show | 26 | HG01168.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.159-1780G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584302 | ||||||
chr1:169584325
|
C | T | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-1803G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584325 | ||||||
chr1:169584328
|
C | T | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-1806G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584328 | ||||||
chr1:169584550
|
C | T | 2 | a0002c0003t0001g0220a0004c0021t0001g0221 | 2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.158+1679G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584550 | ||||||
chr1:169584554
|
C | T | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+1675G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584554 | ||||||
chr1:169584568
|
A | G | 13 | a0004c0040t0002g0301a0004c0040t0003g0289a0004c0059t0001g0300others(10): Show | 13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.158+1661T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584568 | ||||||
chr1:169584623
|
T | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+1606A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584623 | ||||||
chr1:169584658
|
G | T | 1 | a0008c0014t0001g0018 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.158+1571C>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584658 | ||||||
chr1:169584820
|
C | G | 238 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0090others(235): Show | 239 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.158+1409G>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169584820 | ||||||
chr1:169585230
|
T | C | 1 | a0002c0070t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.158+999A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169585230 | ||||||
chr1:169585518
|
T | G | 8 | a0002c0019t0001g0284a0004c0050t0003g0279a0005c0006t0001g0280others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+711A>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169585518 | ||||||
chr1:169585553
|
C | T | 6 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(3): Show | 6 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+676G>A | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169585553 | ||||||
chr1:169585699
|
A | G | 2 | a0003c0022t0004g0016a0007c0041t0008g0017 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.158+530T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169585699 | ||||||
chr1:169585936
|
T | C | 1 | a0011c0036t0003g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.158+293A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169585936 | ||||||
chr1:169585992
|
T | C | 19 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(16): Show | 19 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.158+237A>G | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169585992 | ||||||
chr1:169586129
|
T | A | 2 | a0002c0003t0001g0015a0007c0041t0006g0014 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.158+100A>T | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169586129 | ||||||
chr1:169586129
|
T | TA | 17 | a0004c0021t0006g0295a0004c0040t0002g0301a0004c0059t0001g0300others(14): Show | 17 | HG00735.hp2 HG01168.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.158+99dupT | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169586129 | ||||||
chr1:169586216
|
A | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0015a0004c0007t0003g0012others(1): Show | 4 | HG02886.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+13T>C | F5 | ENSG00000198734.12 | transcript | ENST00000367797.9 | protein_coding | 1/24 | chr1 | 169586216 |