geneid | 29974 |
---|---|
ensemblid | ENSG00000148584.16 |
hgncid | 24086 |
symbol | A1CF |
name | APOBEC1 complementation factor |
refseq_nuc | NM_014576.4 |
refseq_prot | NP_055391.2 |
ensembl_nuc | ENST00000373997.8 |
ensembl_prot | ENSP00000363109.3 |
mane_status | MANE Select |
chr | chr10 |
start | 50799409 |
end | 50885627 |
strand | - |
ver | v1.2 |
region | chr10:50799409-50885627 |
region5000 | chr10:50794409-50890627 |
regionname0 | A1CF_chr10_50799409_50885627 |
regionname5000 | A1CF_chr10_50794409_50890627 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 586 | 325 | 77 | 49 | 145 | 12 | 40 | 111 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002 | 0/0 | 586 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0003 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1761 | 259 | 56 | 45 | 110 | 11 | 35 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0002 | 0/0 | 1761 | 35 | 10 | 1 | 19 | 0 | 5 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0003 | 0/0 | 1761 | 20 | 1 | 3 | 15 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0004 | 0/0 | 1761 | 9 | 8 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0005 | 0/0 | 1761 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0006 | 0/0 | 1761 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0007 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0008 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0009 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0010 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0011 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
c0012 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
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 | 0/1 | 7455 | 100 | 19 | 21 | 46 | 7 | 6 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0002 | 0/0 | 7462 | 54 | 0 | 2 | 43 | 0 | 9 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0003 | 0/0 | 7462 | 45 | 1 | 12 | 23 | 3 | 6 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0004 | 0/0 | 7461 | 35 | 12 | 1 | 19 | 0 | 3 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0005 | 0/0 | 7461 | 32 | 13 | 7 | 2 | 0 | 10 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0006 | 0/0 | 7462 | 8 | 7 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0007 | 0/0 | 7454 | 5 | 1 | 0 | 4 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0008 | 0/0 | 7461 | 4 | 4 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0009 | 0/0 | 7461 | 4 | 4 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0010 | 0/0 | 7461 | 3 | 2 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0011 | 0/0 | 7462 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0012 | 0/0 | 7461 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0013 | 0/0 | 7462 | 2 | 0 | 0 | 0 | 0 | 2 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0014 | 0/0 | 7462 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0015 | 0/0 | 7461 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0016 | 0/0 | 7461 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0017 | 0/0 | 7462 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0018 | 0/0 | 7462 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0019 | 0/0 | 7460 | 2 | 1 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0020 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0021 | 0/0 | 7455 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0022 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0023 | 0/0 | 7455 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0024 | 0/0 | 7456 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0025 | 0/0 | 7456 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0026 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0027 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0028 | 0/0 | 7461 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0029 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0030 | 0/0 | 7462 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0031 | 0/0 | 7462 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0032 | 0/0 | 7462 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0033 | 0/0 | 7461 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0034 | 0/0 | 7461 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0035 | 0/0 | 7462 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0036 | 0/0 | 7462 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0037 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0038 | 0/0 | 7461 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0039 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0040 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0041 | 0/0 | 7462 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0042 | 1/0 | 7461 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0043 | 0/0 | 7461 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0044 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0045 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0046 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0047 | 0/0 | 7454 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0048 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
t0049 | 0/0 | 7461 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
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 | 6 | 0 | 0 | 5 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1761 | 259 | 56 | 45 | 110 | 11 | 35 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0002 | 0/0 | 1761 | 35 | 10 | 1 | 19 | 0 | 5 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0003 | 0/0 | 1761 | 20 | 1 | 3 | 15 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0005 | 0/0 | 1761 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0007 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0008 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0009 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0011 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0012 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0004 | 0/0 | 1761 | 9 | 8 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0006 | 0/0 | 1761 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0003c0010 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 9215 | 80 | 16 | 18 | 33 | 6 | 6 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0002 | 0/0 | 9222 | 53 | 0 | 2 | 42 | 0 | 9 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0003 | 0/0 | 9222 | 45 | 1 | 12 | 23 | 3 | 6 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0005 | 0/0 | 9221 | 31 | 12 | 7 | 2 | 0 | 10 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0007 | 0/0 | 9214 | 3 | 1 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0008 | 0/0 | 9221 | 4 | 4 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0009 | 0/0 | 9221 | 4 | 4 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0010 | 0/0 | 9221 | 3 | 2 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0011 | 0/0 | 9222 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0012 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0014 | 0/0 | 9222 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0015 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0016 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0017 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0019 | 0/0 | 9220 | 2 | 1 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0020 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0021 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0022 | 0/0 | 9215 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0023 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0025 | 0/0 | 9216 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0026 | 0/0 | 9215 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0027 | 0/0 | 9215 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0028 | 0/0 | 9221 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0029 | 0/0 | 9223 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0030 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0031 | 0/0 | 9222 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0032 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0035 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0036 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0037 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0038 | 0/0 | 9221 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0039 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0040 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0041 | 0/0 | 9222 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0042 | 1/0 | 9221 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0043 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0046 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0001t0049 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0002t0004 | 0/0 | 9221 | 33 | 10 | 1 | 19 | 0 | 3 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0002t0013 | 0/0 | 9222 | 2 | 0 | 0 | 0 | 0 | 2 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0003t0001 | 0/0 | 9215 | 17 | 1 | 3 | 12 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0003t0007 | 0/0 | 9214 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0003t0047 | 0/0 | 9214 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0005t0001 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0005t0024 | 0/0 | 9216 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0005t0048 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0007t0005 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0007t0033 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0008t0001 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0008t0017 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0009t0004 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0011t0002 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0001c0012t0034 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0004t0006 | 0/0 | 9222 | 5 | 4 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0004t0018 | 0/0 | 9222 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0004t0044 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0004t0045 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0002c0006t0006 | 0/0 | 9222 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
a0003c0010t0001 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | copy fasta | chr10 | 50794409 | 50890627 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0007g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0008g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0009g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0010g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0016g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0016g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0017g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0019g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0019g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0020g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0021g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0022g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0025g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0026g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0027g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0028g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0029g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0030g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0031g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0032g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0035g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0036g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0037g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0038g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0039g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0040g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0041g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0042g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0043g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0046g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0049g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0013g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0013g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0047g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0005t0024g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0005t0048g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0007t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0007t0033g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0008t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0008t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0009t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0009t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0011t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0012t0034g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0018g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0044g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0045g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0006t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0006t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0006t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0003c0010t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0031 | g0053 | EUR | GBR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0156 | EUR | FIN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00423 | hp1 | a0001 | c0001 | t0032 | g0058 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0083 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00639 | hp1 | a0002 | c0004 | t0006 | g0269 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0265 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01069 | hp2 | a0001 | c0001 | t0028 | g0052 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0251 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0253 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01192 | hp1 | a0001 | c0001 | t0010 | g0097 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0086 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01243 | hp1 | a0001 | c0001 | t0019 | g0241 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0268 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01257 | hp1 | a0001 | c0001 | t0021 | g0110 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0217 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01361 | hp2 | a0001 | c0001 | t0023 | g0114 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01516 | hp2 | a0001 | c0001 | t0022 | g0274 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01891 | hp2 | a0001 | c0001 | t0043 | g0094 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0009 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01981 | hp2 | a0001 | c0001 | t0041 | g0037 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02015 | hp1 | a0001 | c0002 | t0004 | g0080 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02055 | hp2 | a0002 | c0004 | t0006 | g0032 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02080 | hp2 | a0001 | c0001 | t0025 | g0123 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0069 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02145 | hp1 | a0002 | c0004 | t0006 | g0212 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02145 | hp2 | a0001 | c0001 | t0016 | g0040 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0104 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CDX | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | CDX | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02257 | hp1 | a0001 | c0001 | t0017 | g0266 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0248 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02258 | hp2 | a0001 | c0007 | t0005 | g0244 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0279 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02280 | hp2 | a0001 | c0002 | t0004 | g0258 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0223 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02451 | hp2 | a0002 | c0006 | t0006 | g0046 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0075 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0273 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0285 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02615 | hp1 | a0002 | c0004 | t0045 | g0200 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02622 | hp1 | a0002 | c0004 | t0006 | g0226 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02622 | hp2 | a0001 | c0002 | t0004 | g0267 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0031 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0143 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02717 | hp1 | a0001 | c0005 | t0048 | g0209 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02723 | hp2 | a0001 | c0001 | t0019 | g0242 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02735 | hp1 | a0001 | c0002 | t0004 | g0081 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02738 | hp2 | a0001 | c0002 | t0013 | g0088 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02886 | hp2 | a0002 | c0004 | t0018 | g0034 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02895 | hp1 | a0001 | c0009 | t0004 | g0257 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0031 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02897 | hp1 | a0001 | c0009 | t0004 | g0255 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02897 | hp2 | a0001 | c0008 | t0001 | g0039 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02922 | hp2 | a0001 | c0001 | t0037 | g0050 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0092 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02976 | hp1 | a0001 | c0001 | t0039 | g0038 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0093 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0247 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03139 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0250 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03225 | hp2 | a0001 | c0012 | t0034 | g0154 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03453 | hp2 | a0001 | c0005 | t0001 | g0207 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0041 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0252 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0228 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03516 | hp2 | a0001 | c0007 | t0033 | g0245 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0096 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03540 | hp2 | a0002 | c0004 | t0018 | g0153 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03579 | hp2 | a0002 | c0004 | t0006 | g0032 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0280 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03654 | hp2 | a0001 | c0002 | t0013 | g0085 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03669 | hp1 | a0001 | c0001 | t0027 | g0084 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0264 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03710 | hp1 | a0001 | c0001 | t0038 | g0168 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03710 | hp2 | a0001 | c0002 | t0004 | g0082 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03831 | hp1 | a0001 | c0001 | t0029 | g0057 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0282 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0278 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03927 | hp2 | a0001 | c0001 | t0026 | g0054 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0107 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0281 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0275 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0144 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0256 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18906 | hp1 | a0001 | c0008 | t0017 | g0042 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18906 | hp2 | a0002 | c0006 | t0006 | g0044 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18939 | hp2 | a0001 | c0003 | t0047 | g0219 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18946 | hp2 | a0001 | c0011 | t0002 | g0184 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18950 | hp2 | a0001 | c0001 | t0030 | g0229 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18970 | hp2 | a0003 | c0010 | t0001 | g0136 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18974 | hp2 | a0001 | c0003 | t0007 | g0231 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18977 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18984 | hp1 | a0001 | c0001 | t0036 | g0182 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18991 | hp1 | a0001 | c0001 | t0049 | g0167 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19004 | hp2 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19007 | hp1 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19011 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19012 | hp1 | a0001 | c0001 | t0046 | g0124 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0249 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19060 | hp2 | a0001 | c0002 | t0004 | g0105 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19065 | hp2 | a0001 | c0001 | t0020 | g0112 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19070 | hp1 | a0001 | c0003 | t0007 | g0232 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19072 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19072 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19074 | hp2 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19076 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19077 | hp2 | a0001 | c0001 | t0035 | g0155 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19080 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19083 | hp2 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19091 | hp2 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19240 | hp2 | a0002 | c0006 | t0006 | g0045 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20129 | hp1 | a0002 | c0004 | t0044 | g0049 | AFR | ASW | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ASW | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | TSI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | GIH | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0087 | SAS | GIH | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0254 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02559 | hp1 | a0001 | c0005 | t0024 | g0208 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02559 | hp2 | a0001 | c0001 | t0015 | g0095 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03471 | hp1 | a0001 | c0001 | t0040 | g0047 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18955 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0042 | g0048 | REF | REF | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50806851
|
C | T | 1 | a0002 | 12 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
missense_variant | MODERATE | c.1639G>A | p.Val547Met | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1779/9221 | 1639/1761 | 547/586 | chr10 | 50806851 | ||
chr10:50811146
|
A | G | 1 | a0003 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.1354T>C | p.Trp452Arg | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/13 | 1494/9221 | 1354/1761 | 452/586 | chr10 | 50811146 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50806834
|
G | C | 1 | a0001c0003 | 20 | HG00280.hp2 HG00558.hp2 HG01346.hp1 others(17): Show |
synonymous_variant | LOW | c.1656C>G | p.Leu552Leu | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1796/9221 | 1656/1761 | 552/586 | chr10 | 50806834 | ||
chr10:50809991
|
C | T | 1 | a0001c0009 | 2 | HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.1512G>A | p.Thr504Thr | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/13 | 1652/9221 | 1512/1761 | 504/586 | chr10 | 50809991 | ||
chr10:50813938
|
G | A | 3 | a0001c0002a0001c0009a0001c0012 | 38 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
synonymous_variant | LOW | c.1242C>T | p.Leu414Leu | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/13 | 1382/9221 | 1242/1761 | 414/586 | chr10 | 50813938 | ||
chr10:50816244
|
T | G | 1 | a0001c0011 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.903A>C | p.Ala301Ala | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/13 | 1043/9221 | 903/1761 | 301/586 | chr10 | 50816244 | ||
chr10:50836093
|
C | T | 2 | a0001c0008a0002c0006 | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
synonymous_variant | LOW | c.585G>A | p.Ala195Ala | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/13 | 725/9221 | 585/1761 | 195/586 | chr10 | 50836093 | ||
chr10:50836150
|
G | T | 1 | a0001c0007 | 2 | HG02258.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.528C>A | p.Thr176Thr | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/13 | 668/9221 | 528/1761 | 176/586 | chr10 | 50836150 | ||
chr10:50836216
|
C | T | 1 | a0001c0005 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.462G>A | p.Ser154Ser | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/13 | 602/9221 | 462/1761 | 154/586 | chr10 | 50836216 | ||
chr10:50859911
|
T | G | 1 | a0001c0012 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.30A>C | p.Gly10Gly | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/13 | 170/9221 | 30/1761 | 10/586 | chr10 | 50859911 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50799749
|
G | C | 1 | a0001c0001t0026 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6980C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6980 | chr10 | 50799749 | |||||
chr10:50799836
|
C | T | 2 | a0001c0005t0024a0001c0005t0048 | 2 | HG02559.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6893G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6893 | chr10 | 50799836 | |||||
chr10:50799874
|
A | G | 12 | a0001c0001t0016a0001c0001t0017a0001c0002t0004others(9): Show | 54 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*6855T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6855 | chr10 | 50799874 | |||||
chr10:50800042
|
A | G | 1 | a0001c0001t0031 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6687T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6687 | chr10 | 50800042 | |||||
chr10:50800083
|
T | G | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*6646A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6646 | chr10 | 50800083 | |||||
chr10:50800104
|
A | T | 1 | a0001c0003t0047 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6625T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6625 | chr10 | 50800104 | |||||
chr10:50800240
|
C | T | 1 | a0001c0001t0019 | 2 | HG01243.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6489G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6489 | chr10 | 50800240 | |||||
chr10:50800634
|
G | A | 4 | a0001c0001t0037a0001c0001t0039a0001c0001t0040others(1): Show | 4 | HG01981.hp2 HG02922.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6095C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6095 | chr10 | 50800634 | |||||
chr10:50800699
|
G | A | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*6030C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6030 | chr10 | 50800699 | |||||
chr10:50800716
|
G | A | 5 | a0001c0001t0002a0001c0001t0035a0001c0001t0036others(2): Show | 57 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*6013C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6013 | chr10 | 50800716 | |||||
chr10:50800797
|
G | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*5932C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5932 | chr10 | 50800797 | |||||
chr10:50800898
|
A | T | 6 | a0001c0001t0016a0002c0004t0006a0002c0004t0018others(3): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5831T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5831 | chr10 | 50800898 | |||||
chr10:50800933
|
C | T | 1 | a0002c0004t0018 | 2 | HG02886.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5796G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5796 | chr10 | 50800933 | |||||
chr10:50800934
|
G | A | 1 | a0001c0001t0011 | 2 | HG02965.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5795C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5795 | chr10 | 50800934 | |||||
chr10:50800971
|
T | A | 1 | a0001c0001t0037 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5758A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5758 | chr10 | 50800971 | |||||
chr10:50801395
|
T | A | 7 | a0001c0001t0017a0001c0008t0017a0002c0004t0006others(4): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5334A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5334 | chr10 | 50801395 | |||||
chr10:50801491
|
G | A | 1 | a0001c0001t0041 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5238C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5238 | chr10 | 50801491 | |||||
chr10:50801883
|
T | C | 3 | a0001c0001t0012a0001c0001t0028a0001c0007t0033 | 4 | HG01069.hp2 HG02451.hp1 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4846A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4846 | chr10 | 50801883 | |||||
chr10:50802039
|
G | A | 1 | a0002c0004t0045 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4690C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4690 | chr10 | 50802039 | |||||
chr10:50802043
|
A | G | 5 | a0001c0001t0016a0001c0002t0004a0001c0002t0013others(2): Show | 40 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4686T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4686 | chr10 | 50802043 | |||||
chr10:50802069
|
C | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*4660G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4660 | chr10 | 50802069 | |||||
chr10:50802159
|
C | T | 5 | a0001c0001t0002a0001c0001t0035a0001c0001t0036others(2): Show | 57 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4570G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4570 | chr10 | 50802159 | |||||
chr10:50802194
|
C | T | 1 | a0001c0001t0008 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4535G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4535 | chr10 | 50802194 | |||||
chr10:50802340
|
G | A | 1 | a0001c0001t0010 | 3 | HG01192.hp1 HG02630.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4389C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4389 | chr10 | 50802340 | |||||
chr10:50802678
|
CTTAGTG | C | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4045_*4050delCACT others(2): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4045 | chr10 | 50802678 | |||||
chr10:50803237
|
C | T | 1 | a0001c0001t0030 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3492G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3492 | chr10 | 50803237 | |||||
chr10:50803269
|
G | GT | 16 | a0001c0001t0014a0001c0001t0017a0001c0001t0025others(13): Show | 25 | HG00639.hp1 HG01981.hp2 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3459dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3459 | chr10 | 50803269 | |||||
chr10:50803269
|
G | T | 1 | a0001c0001t0023 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3460C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3460 | chr10 | 50803269 | |||||
chr10:50803291
|
C | T | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(8): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3438G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3438 | chr10 | 50803291 | |||||
chr10:50803387
|
G | A | 1 | a0001c0001t0027 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3342C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3342 | chr10 | 50803387 | |||||
chr10:50803391
|
C | T | 2 | a0001c0001t0037a0001c0001t0039 | 2 | HG02922.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3338G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3338 | chr10 | 50803391 | |||||
chr10:50803436
|
A | G | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*3293T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3293 | chr10 | 50803436 | |||||
chr10:50803585
|
A | C | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3144T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3144 | chr10 | 50803585 | |||||
chr10:50803619
|
A | G | 2 | a0001c0001t0028a0001c0007t0033 | 2 | HG01069.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3110T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3110 | chr10 | 50803619 | |||||
chr10:50803947
|
A | G | 1 | a0001c0001t0022 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2782T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2782 | chr10 | 50803947 | |||||
chr10:50803965
|
G | A | 1 | a0001c0001t0032 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2764C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2764 | chr10 | 50803965 | |||||
chr10:50804022
|
G | A | 1 | a0001c0001t0009 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2707C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2707 | chr10 | 50804022 | |||||
chr10:50804305
|
C | T | 1 | a0001c0001t0021 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2424G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2424 | chr10 | 50804305 | |||||
chr10:50804315
|
A | AT | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(8): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2413dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2413 | chr10 | 50804315 | |||||
chr10:50804519
|
C | T | 1 | a0001c0001t0038 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2210G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2210 | chr10 | 50804519 | |||||
chr10:50804661
|
G | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2068C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2068 | chr10 | 50804661 | |||||
chr10:50804764
|
G | T | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1965C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1965 | chr10 | 50804764 | |||||
chr10:50804865
|
A | T | 1 | a0001c0001t0037 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1864T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1864 | chr10 | 50804865 | |||||
chr10:50805008
|
G | A | 3 | a0001c0002t0004a0001c0002t0013a0001c0009t0004 | 37 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1721C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1721 | chr10 | 50805008 | |||||
chr10:50805422
|
C | T | 1 | a0002c0004t0044 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1307 | chr10 | 50805422 | |||||
chr10:50805438
|
G | A | 1 | a0001c0001t0035 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1291 | chr10 | 50805438 | |||||
chr10:50805472
|
T | C | 1 | a0001c0001t0036 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1257 | chr10 | 50805472 | |||||
chr10:50805613
|
C | T | 1 | a0001c0001t0020 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1116G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1116 | chr10 | 50805613 | |||||
chr10:50805968
|
G | T | 1 | a0001c0001t0028 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*761C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 761 | chr10 | 50805968 | |||||
chr10:50806119
|
G | C | 2 | a0001c0001t0009a0001c0001t0043 | 5 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 610 | chr10 | 50806119 | |||||
chr10:50806180
|
A | C | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*549T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 549 | chr10 | 50806180 | |||||
chr10:50806289
|
T | C | 8 | a0001c0001t0016a0001c0001t0017a0001c0008t0017others(5): Show | 16 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*440A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 440 | chr10 | 50806289 | |||||
chr10:50806297
|
A | G | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*432T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 432 | chr10 | 50806297 | |||||
chr10:50806607
|
G | A | 1 | a0001c0001t0046 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 122 | chr10 | 50806607 | |||||
chr10:50806672
|
CT | C | 6 | a0001c0001t0007a0001c0001t0019a0001c0001t0049others(3): Show | 10 | HG01243.hp1 HG02717.hp1 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*56delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 56 | chr10 | 50806672 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50807085
|
C | T | 1 | a0001c0001t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1610-205G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807085 | ||||||
chr10:50807146
|
C | T | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1610-266G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807146 | ||||||
chr10:50807215
|
G | T | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(255): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1610-335C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807215 | ||||||
chr10:50807300
|
G | A | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1610-420C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807300 | ||||||
chr10:50807411
|
G | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0008t0001g0039 | 3 | HG02109.hp1 HG02486.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1610-531C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807411 | ||||||
chr10:50807564
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0008t0001g0039 | 3 | HG02109.hp1 HG02486.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1610-684C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807564 | ||||||
chr10:50807672
|
G | A | 1 | a0001c0001t0005g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1610-792C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807672 | ||||||
chr10:50808105
|
A | G | 246 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(243): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1610-1225T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808105 | ||||||
chr10:50808118
|
T | C | 1 | a0002c0004t0006g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1610-1238A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808118 | ||||||
chr10:50808246
|
C | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1610-1366G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808246 | ||||||
chr10:50808856
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1609+1038A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808856 | ||||||
chr10:50809127
|
G | T | 7 | a0001c0001t0005g0201a0001c0001t0005g0202a0001c0001t0005g0206others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+767C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809127 | ||||||
chr10:50809238
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(96): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1609+656T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809238 | ||||||
chr10:50809321
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1609+573G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809321 | ||||||
chr10:50809332
|
C | A | 6 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1609+562G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809332 | ||||||
chr10:50809791
|
C | T | 1 | a0001c0001t0008g0006 | 3 | HG02258.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1609+103G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809791 | ||||||
chr10:50809877
|
G | A | 36 | a0001c0001t0003g0008a0001c0001t0003g0012a0001c0001t0003g0013others(33): Show | 46 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1609+17C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809877 | ||||||
chr10:50810338
|
C | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(95): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1461-296G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810338 | ||||||
chr10:50810355
|
G | C | 90 | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0007others(87): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1461-313C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810355 | ||||||
chr10:50810457
|
A | G | 32 | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(29): Show | 37 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1461-415T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810457 | ||||||
chr10:50810463
|
G | A | 2 | a0001c0001t0005g0143a0001c0001t0005g0144 | 2 | HG02683.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1461-421C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810463 | ||||||
chr10:50810481
|
G | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(95): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1461-439C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810481 | ||||||
chr10:50810503
|
A | G | 2 | a0001c0001t0028g0052a0001c0007t0033g0245 | 2 | HG01069.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1461-461T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810503 | ||||||
chr10:50810578
|
G | A | 1 | a0001c0007t0033g0245 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1460+462C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810578 | ||||||
chr10:50810620
|
G | A | 3 | a0001c0002t0004g0160a0001c0003t0001g0109a0001c0003t0001g0222 | 3 | HG02055.hp1 NA18945.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1460+420C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810620 | ||||||
chr10:50810881
|
C | T | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1460+159G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810881 | ||||||
chr10:50810983
|
T | G | 7 | a0002c0004t0006g0032a0002c0004t0006g0212a0002c0004t0006g0226others(4): Show | 8 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+57A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810983 | ||||||
chr10:50811287
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(283): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1324-111G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811287 | ||||||
chr10:50811298
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1324-122T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811298 | ||||||
chr10:50811304
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1324-128A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811304 | ||||||
chr10:50811405
|
T | C | 1 | a0001c0001t0005g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1324-229A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811405 | ||||||
chr10:50811485
|
A | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0027others(90): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1324-309T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811485 | ||||||
chr10:50811532
|
C | T | 1 | a0001c0001t0003g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1324-356G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811532 | ||||||
chr10:50811600
|
C | T | 6 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-424G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811600 | ||||||
chr10:50811613
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1324-437T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811613 | ||||||
chr10:50811668
|
G | C | 1 | a0002c0004t0044g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1324-492C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811668 | ||||||
chr10:50811742
|
C | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(255): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1324-566G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811742 | ||||||
chr10:50811909
|
T | G | 1 | a0001c0001t0041g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1324-733A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811909 | ||||||
chr10:50811941
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1324-765T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811941 | ||||||
chr10:50811954
|
G | A | 1 | a0001c0003t0007g0232 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1324-778C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811954 | ||||||
chr10:50811969
|
T | C | 6 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-793A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811969 | ||||||
chr10:50812043
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1324-867T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812043 | ||||||
chr10:50812164
|
T | C | 90 | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0007others(87): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1324-988A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812164 | ||||||
chr10:50812251
|
G | A | 1 | a0001c0001t0032g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1324-1075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812251 | ||||||
chr10:50812341
|
C | T | 1 | a0001c0002t0004g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1324-1165G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812341 | ||||||
chr10:50812359
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1324-1183C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812359 | ||||||
chr10:50812526
|
C | T | 6 | a0001c0001t0017g0266a0001c0001t0037g0050a0001c0001t0039g0038others(3): Show | 6 | HG01981.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1331G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812526 | ||||||
chr10:50812613
|
T | C | 1 | a0001c0001t0043g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1323+1244A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812613 | ||||||
chr10:50812749
|
C | T | 32 | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(29): Show | 37 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1323+1108G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812749 | ||||||
chr10:50812880
|
T | A | 4 | a0001c0001t0001g0090a0001c0001t0017g0266a0001c0001t0040g0047others(1): Show | 4 | HG02257.hp1 HG03471.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+977A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812880 | ||||||
chr10:50812893
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(96): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1323+964C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812893 | ||||||
chr10:50812964
|
A | C | 2 | a0001c0001t0012g0075a0001c0001t0012g0223 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1323+893T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812964 | ||||||
chr10:50812976
|
C | T | 2 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+881G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812976 | ||||||
chr10:50812981
|
A | G | 2 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+876T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812981 | ||||||
chr10:50813273
|
A | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0099a0001c0001t0001g0147others(2): Show | 6 | NA18947.hp2 NA18962.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+584T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50813273 | ||||||
chr10:50813499
|
C | A | 8 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(5): Show | 9 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1323+358G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50813499 | ||||||
chr10:50813654
|
A | T | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1323+203T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50813654 | ||||||
chr10:50814086
|
A | G | 1 | a0001c0001t0005g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1142-48T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814086 | ||||||
chr10:50814156
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1142-118A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814156 | ||||||
chr10:50814208
|
C | T | 1 | a0001c0001t0009g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1142-170G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814208 | ||||||
chr10:50814276
|
C | T | 1 | a0001c0003t0001g0137 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1142-238G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814276 | ||||||
chr10:50814313
|
C | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0027others(90): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1142-275G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814313 | ||||||
chr10:50814344
|
A | G | 13 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0002g0175others(10): Show | 13 | HG00438.hp2 HG00558.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1142-306T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814344 | ||||||
chr10:50814707
|
A | G | 1 | a0001c0001t0032g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1142-669T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814707 | ||||||
chr10:50814885
|
A | G | 53 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0027others(50): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1142-847T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814885 | ||||||
chr10:50815113
|
G | T | 1 | a0001c0001t0003g0270 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1141+893C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815113 | ||||||
chr10:50815133
|
C | T | 3 | a0001c0001t0017g0266a0001c0001t0040g0047a0001c0008t0017g0042 | 3 | HG02257.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1141+873G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815133 | ||||||
chr10:50815394
|
T | C | 2 | a0001c0001t0005g0143a0001c0001t0005g0144 | 2 | HG02683.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1141+612A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815394 | ||||||
chr10:50815521
|
T | A | 1 | a0001c0001t0003g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1141+485A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815521 | ||||||
chr10:50815728
|
T | C | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1141+278A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815728 | ||||||
chr10:50815888
|
A | G | 1 | a0001c0003t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1141+118T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815888 | ||||||
chr10:50815930
|
A | G | 1 | a0001c0001t0003g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1141+76T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815930 | ||||||
chr10:50816307
|
C | T | 1 | a0001c0001t0005g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.868-28G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816307 | ||||||
chr10:50816308
|
G | A | 247 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(244): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.868-29C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816308 | ||||||
chr10:50816354
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.868-75A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816354 | ||||||
chr10:50816459
|
G | A | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.868-180C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816459 | ||||||
chr10:50816670
|
A | G | 36 | a0001c0001t0005g0010a0001c0001t0016g0040a0001c0001t0016g0041others(33): Show | 43 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.868-391T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816670 | ||||||
chr10:50816728
|
T | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(96): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.868-449A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816728 | ||||||
chr10:50816782
|
C | T | 4 | a0001c0001t0005g0107a0001c0001t0005g0262a0001c0001t0005g0273others(1): Show | 4 | HG00438.hp1 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-503G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816782 | ||||||
chr10:50816830
|
T | C | 13 | a0001c0001t0017g0266a0001c0008t0017g0042a0002c0004t0006g0032others(10): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.868-551A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816830 | ||||||
chr10:50817113
|
G | A | 93 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0027others(90): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.868-834C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817113 | ||||||
chr10:50817296
|
A | C | 1 | a0001c0001t0002g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.868-1017T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817296 | ||||||
chr10:50817493
|
G | A | 13 | a0001c0001t0017g0266a0001c0008t0017g0042a0002c0004t0006g0032others(10): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.868-1214C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817493 | ||||||
chr10:50817596
|
G | A | 8 | a0002c0004t0006g0032a0002c0004t0006g0212a0002c0004t0006g0226others(5): Show | 9 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-1317C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817596 | ||||||
chr10:50818055
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(94): Show | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.868-1776G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818055 | ||||||
chr10:50818191
|
C | T | 2 | a0001c0001t0016g0040a0001c0001t0016g0041 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.868-1912G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818191 | ||||||
chr10:50818220
|
G | C | 1 | a0001c0007t0033g0245 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.868-1941C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818220 | ||||||
chr10:50818352
|
T | A | 93 | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0007others(90): Show | 112 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.868-2073A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818352 | ||||||
chr10:50818440
|
A | G | 1 | a0001c0001t0040g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+2112T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818440 | ||||||
chr10:50818518
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.867+2034G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818518 | ||||||
chr10:50818612
|
C | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0216 | 2 | NA18987.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.867+1940G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818612 | ||||||
chr10:50818711
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.867+1841C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818711 | ||||||
chr10:50818804
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.867+1748G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818804 | ||||||
chr10:50818956
|
C | G | 2 | a0001c0001t0028g0052a0001c0007t0033g0245 | 2 | HG01069.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.867+1596G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818956 | ||||||
chr10:50818978
|
A | G | 66 | a0001c0001t0001g0140a0001c0001t0002g0051a0001c0001t0002g0162others(63): Show | 77 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.867+1574T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818978 | ||||||
chr10:50819061
|
G | C | 4 | a0001c0001t0019g0241a0001c0001t0019g0242a0001c0001t0041g0037others(1): Show | 4 | HG01243.hp1 HG01981.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+1491C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819061 | ||||||
chr10:50819137
|
T | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.867+1415A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819137 | ||||||
chr10:50819158
|
C | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0130others(1): Show | 4 | HG01167.hp2 HG02109.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+1394G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819158 | ||||||
chr10:50819250
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.867+1302C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819250 | ||||||
chr10:50819291
|
C | T | 1 | a0001c0001t0040g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+1261G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819291 | ||||||
chr10:50819292
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(57): Show | 69 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.867+1260C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819292 | ||||||
chr10:50819457
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.867+1095G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819457 | ||||||
chr10:50819491
|
C | T | 2 | a0001c0001t0015g0095a0001c0001t0015g0096 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.867+1061G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819491 | ||||||
chr10:50819494
|
T | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0210a0001c0001t0001g0213others(2): Show | 6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.867+1058A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819494 | ||||||
chr10:50819551
|
C | T | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.867+1001G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819551 | ||||||
chr10:50819566
|
G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+986C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819566 | ||||||
chr10:50819654
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0027g0084 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.867+898T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819654 | ||||||
chr10:50819781
|
G | C | 1 | a0001c0008t0017g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.867+771C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819781 | ||||||
chr10:50819835
|
T | C | 7 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.867+717A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819835 | ||||||
chr10:50819943
|
C | A | 9 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+609G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819943 | ||||||
chr10:50819990
|
T | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+562A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819990 | ||||||
chr10:50820208
|
C | T | 1 | a0002c0006t0006g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.867+344G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50820208 | ||||||
chr10:50820453
|
G | A | 5 | a0001c0008t0001g0039a0002c0004t0044g0049a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+99C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50820453 | ||||||
chr10:50820692
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770-43C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820692 | ||||||
chr10:50820797
|
A | G | 9 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-148T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820797 | ||||||
chr10:50820889
|
G | A | 1 | a0001c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.770-240C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820889 | ||||||
chr10:50820933
|
T | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.770-284A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820933 | ||||||
chr10:50821359
|
C | T | 9 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-710G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821359 | ||||||
chr10:50821442
|
A | G | 1 | a0001c0001t0039g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.770-793T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821442 | ||||||
chr10:50821535
|
A | C | 1 | a0001c0001t0002g0176 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.770-886T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821535 | ||||||
chr10:50821541
|
A | AT | 130 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(127): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.770-893dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821541 | ||||||
chr10:50821757
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.770-1108C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821757 | ||||||
chr10:50821807
|
G | C | 4 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-1158C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821807 | ||||||
chr10:50821966
|
T | G | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.770-1317A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821966 | ||||||
chr10:50822075
|
C | T | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.770-1426G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822075 | ||||||
chr10:50822105
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.770-1456A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822105 | ||||||
chr10:50822132
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0189a0001c0001t0001g0234others(3): Show | 9 | HG00738.hp1 HG01258.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.770-1483T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822132 | ||||||
chr10:50822370
|
G | A | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-1721C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822370 | ||||||
chr10:50822465
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.770-1816C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822465 | ||||||
chr10:50822497
|
C | T | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.770-1848G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822497 | ||||||
chr10:50822500
|
G | A | 1 | a0001c0001t0015g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.770-1851C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822500 | ||||||
chr10:50822594
|
T | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0198 | 3 | HG02083.hp1 NA18986.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.770-1945A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822594 | ||||||
chr10:50822746
|
A | T | 1 | a0001c0007t0033g0245 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.770-2097T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822746 | ||||||
chr10:50822756
|
G | A | 1 | a0001c0001t0016g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.770-2107C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822756 | ||||||
chr10:50822778
|
C | T | 1 | a0001c0001t0022g0274 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.770-2129G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822778 | ||||||
chr10:50822817
|
C | T | 1 | a0001c0001t0011g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.770-2168G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822817 | ||||||
chr10:50822826
|
A | C | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.770-2177T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822826 | ||||||
chr10:50822855
|
C | T | 2 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.770-2206G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822855 | ||||||
chr10:50822885
|
C | A | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.770-2236G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822885 | ||||||
chr10:50823008
|
G | A | 1 | a0001c0001t0021g0110 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.770-2359C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823008 | ||||||
chr10:50823283
|
G | A | 19 | a0001c0001t0001g0220a0001c0001t0030g0229a0001c0003t0001g0009others(16): Show | 22 | HG00280.hp2 HG00558.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.770-2634C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823283 | ||||||
chr10:50823490
|
C | A | 2 | a0001c0002t0004g0073a0001c0002t0004g0079 | 2 | NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.770-2841G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823490 | ||||||
chr10:50823533
|
C | T | 1 | a0001c0001t0003g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.770-2884G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823533 | ||||||
chr10:50823534
|
G | C | 21 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(18): Show | 24 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.770-2885C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823534 | ||||||
chr10:50823648
|
G | A | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-2999C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823648 | ||||||
chr10:50823735
|
A | G | 1 | a0001c0001t0002g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.770-3086T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823735 | ||||||
chr10:50823863
|
G | A | 2 | a0002c0004t0006g0212a0002c0004t0006g0226 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.770-3214C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823863 | ||||||
chr10:50823903
|
G | A | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-3254C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823903 | ||||||
chr10:50823968
|
C | G | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-3319G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823968 | ||||||
chr10:50824153
|
G | A | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.770-3504C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824153 | ||||||
chr10:50824284
|
C | T | 1 | a0001c0001t0032g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.770-3635G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824284 | ||||||
chr10:50824285
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.770-3636C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824285 | ||||||
chr10:50824350
|
T | C | 49 | a0001c0001t0001g0276a0001c0001t0003g0008a0001c0001t0003g0018others(46): Show | 60 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.770-3701A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824350 | ||||||
chr10:50824412
|
G | T | 1 | a0001c0001t0015g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.769+3719C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824412 | ||||||
chr10:50824645
|
GGCATGTA others(3): Show |
G | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+3476_769+3485d others(12): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824645 | ||||||
chr10:50824709
|
C | T | 1 | a0001c0003t0001g0137 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.769+3422G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824709 | ||||||
chr10:50824917
|
C | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+3214G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824917 | ||||||
chr10:50824949
|
C | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+3182G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824949 | ||||||
chr10:50825233
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.769+2898G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825233 | ||||||
chr10:50825450
|
T | A | 1 | a0001c0001t0003g0013 | 2 | NA18945.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.769+2681A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825450 | ||||||
chr10:50825453
|
G | A | 5 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+2678C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825453 | ||||||
chr10:50825479
|
A | G | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769+2652T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825479 | ||||||
chr10:50826129
|
T | C | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+2002A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826129 | ||||||
chr10:50826428
|
A | G | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.769+1703T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826428 | ||||||
chr10:50826446
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.769+1685C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826446 | ||||||
chr10:50826480
|
C | T | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+1651G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826480 | ||||||
chr10:50826533
|
G | C | 7 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+1598C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826533 | ||||||
chr10:50826560
|
A | G | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.769+1571T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826560 | ||||||
chr10:50826579
|
T | G | 1 | a0002c0004t0044g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.769+1552A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826579 | ||||||
chr10:50826860
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.769+1271A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826860 | ||||||
chr10:50826869
|
C | T | 1 | a0001c0002t0004g0078 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.769+1262G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826869 | ||||||
chr10:50826910
|
T | C | 1 | a0001c0001t0005g0264 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+1221A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826910 | ||||||
chr10:50827088
|
C | A | 1 | a0001c0001t0002g0185 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.769+1043G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827088 | ||||||
chr10:50827313
|
A | G | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.769+818T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827313 | ||||||
chr10:50827410
|
G | T | 1 | a0001c0002t0004g0105 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.769+721C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827410 | ||||||
chr10:50827485
|
C | A | 21 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(18): Show | 24 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.769+646G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827485 | ||||||
chr10:50827506
|
A | T | 2 | a0001c0001t0003g0059a0001c0001t0003g0061 | 2 | HG02074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.769+625T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827506 | ||||||
chr10:50827812
|
G | T | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.769+319C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827812 | ||||||
chr10:50827870
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.769+261T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827870 | ||||||
chr10:50827932
|
A | G | 12 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.769+199T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827932 | ||||||
chr10:50827955
|
T | C | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.769+176A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827955 | ||||||
chr10:50827989
|
G | A | 3 | a0001c0001t0020g0112a0001c0002t0004g0019a0001c0002t0004g0105 | 4 | HG00621.hp1 NA19011.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+142C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827989 | ||||||
chr10:50828002
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.769+129T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50828002 | ||||||
chr10:50828803
|
G | C | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.605-508C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828803 | ||||||
chr10:50828813
|
A | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-518T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828813 | ||||||
chr10:50828907
|
A | G | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-612T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828907 | ||||||
chr10:50828945
|
A | C | 1 | a0001c0001t0005g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.605-650T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828945 | ||||||
chr10:50829091
|
A | G | 7 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.605-796T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829091 | ||||||
chr10:50829247
|
G | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.605-952C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829247 | ||||||
chr10:50829268
|
T | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.605-973A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829268 | ||||||
chr10:50829345
|
G | T | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-1050C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829345 | ||||||
chr10:50829399
|
G | A | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.605-1104C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829399 | ||||||
chr10:50829666
|
C | G | 1 | a0001c0001t0002g0179 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.605-1371G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829666 | ||||||
chr10:50829836
|
G | A | 21 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(18): Show | 24 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.605-1541C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829836 | ||||||
chr10:50829944
|
C | G | 1 | a0001c0001t0038g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.605-1649G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829944 | ||||||
chr10:50830224
|
G | T | 1 | a0001c0001t0005g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.605-1929C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830224 | ||||||
chr10:50830370
|
G | A | 4 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-2075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830370 | ||||||
chr10:50830485
|
A | T | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-2190T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830485 | ||||||
chr10:50830563
|
AAAATGAA others(6): Show |
A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-2281_605-2269d others(15): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830563 | ||||||
chr10:50830685
|
C | T | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.605-2390G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830685 | ||||||
chr10:50830702
|
T | C | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG02083.hp2 NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.605-2407A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830702 | ||||||
chr10:50830806
|
G | T | 19 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(16): Show | 26 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.605-2511C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830806 | ||||||
chr10:50830876
|
A | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0194 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.605-2581T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830876 | ||||||
chr10:50830905
|
A | AAAACAGA others(5): Show |
2 | a0001c0002t0004g0019a0001c0002t0004g0105 | 3 | HG00621.hp1 NA19011.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.605-2622_605-2611d others(14): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830905 | ||||||
chr10:50831007
|
A | T | 2 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.605-2712T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831007 | ||||||
chr10:50831174
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0099 | 3 | NA18947.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.605-2879C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831174 | ||||||
chr10:50831262
|
A | G | 1 | a0001c0001t0002g0178 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.605-2967T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831262 | ||||||
chr10:50831283
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0037g0050 | 2 | HG00673.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.605-2988G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831283 | ||||||
chr10:50831305
|
A | G | 14 | a0001c0001t0001g0276a0001c0001t0003g0033a0001c0001t0003g0259others(11): Show | 15 | HG00438.hp1 HG01516.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.605-3010T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831305 | ||||||
chr10:50831451
|
G | A | 4 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-3156C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831451 | ||||||
chr10:50831467
|
A | G | 19 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.605-3172T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831467 | ||||||
chr10:50831539
|
A | T | 1 | a0001c0001t0002g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.605-3244T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831539 | ||||||
chr10:50831588
|
C | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-3293G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831588 | ||||||
chr10:50831589
|
G | A | 1 | a0001c0001t0007g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.605-3294C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831589 | ||||||
chr10:50831723
|
C | T | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.605-3428G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831723 | ||||||
chr10:50831726
|
C | T | 1 | a0001c0001t0031g0053 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.605-3431G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831726 | ||||||
chr10:50831795
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.605-3500G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831795 | ||||||
chr10:50831852
|
C | A | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.605-3557G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831852 | ||||||
chr10:50831887
|
G | A | 44 | a0001c0001t0001g0276a0001c0001t0003g0018a0001c0001t0003g0033others(41): Show | 53 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.605-3592C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831887 | ||||||
chr10:50831940
|
T | C | 18 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(15): Show | 21 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.605-3645A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831940 | ||||||
chr10:50832047
|
G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-3752C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832047 | ||||||
chr10:50832114
|
C | T | 1 | a0001c0003t0001g0230 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.605-3819G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832114 | ||||||
chr10:50832185
|
T | C | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+3889A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832185 | ||||||
chr10:50832227
|
G | T | 2 | a0001c0001t0002g0027a0001c0001t0035g0155 | 3 | HG00621.hp2 NA19065.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.604+3847C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832227 | ||||||
chr10:50832253
|
G | A | 7 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.604+3821C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832253 | ||||||
chr10:50832390
|
A | C | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+3684T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832390 | ||||||
chr10:50832494
|
C | T | 32 | a0001c0001t0001g0074a0001c0001t0005g0251a0001c0001t0005g0253others(29): Show | 36 | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.604+3580G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832494 | ||||||
chr10:50832505
|
A | G | 1 | a0002c0006t0006g0044 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604+3569T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832505 | ||||||
chr10:50832569
|
T | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+3505A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832569 | ||||||
chr10:50832606
|
T | G | 1 | a0001c0001t0002g0186 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.604+3468A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832606 | ||||||
chr10:50832700
|
A | T | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+3374T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832700 | ||||||
chr10:50832839
|
C | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+3235G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832839 | ||||||
chr10:50832867
|
GT | G | 15 | a0001c0001t0003g0014a0001c0001t0008g0006a0001c0001t0008g0098others(12): Show | 19 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.604+3206delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832867 | ||||||
chr10:50832873
|
T | G | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+3201A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832873 | ||||||
chr10:50832918
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.604+3156A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832918 | ||||||
chr10:50833143
|
A | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2931T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833143 | ||||||
chr10:50833298
|
G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2776C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833298 | ||||||
chr10:50833477
|
G | C | 1 | a0001c0002t0004g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.604+2597C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833477 | ||||||
chr10:50833661
|
G | T | 1 | a0001c0001t0002g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.604+2413C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833661 | ||||||
chr10:50834010
|
T | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(61): Show | 78 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.604+2064A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834010 | ||||||
chr10:50834107
|
C | T | 2 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.604+1967G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834107 | ||||||
chr10:50834266
|
A | G | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+1808T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834266 | ||||||
chr10:50834479
|
G | T | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+1595C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834479 | ||||||
chr10:50834503
|
G | C | 1 | a0002c0004t0044g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604+1571C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834503 | ||||||
chr10:50834592
|
G | C | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.604+1482C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834592 | ||||||
chr10:50834629
|
A | G | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+1445T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834629 | ||||||
chr10:50834680
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.604+1394G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834680 | ||||||
chr10:50834690
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+1384C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834690 | ||||||
chr10:50834755
|
T | C | 4 | a0001c0002t0004g0071a0001c0002t0004g0076a0001c0002t0004g0077others(1): Show | 4 | HG02015.hp1 NA18977.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+1319A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834755 | ||||||
chr10:50834768
|
G | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.604+1306C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834768 | ||||||
chr10:50835087
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(16): Show | 26 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.604+987T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835087 | ||||||
chr10:50835111
|
A | G | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+963T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835111 | ||||||
chr10:50835133
|
A | G | 2 | a0001c0001t0009g0158a0001c0001t0009g0159 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.604+941T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835133 | ||||||
chr10:50835230
|
A | G | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.604+844T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835230 | ||||||
chr10:50835355
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 72 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.604+719C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835355 | ||||||
chr10:50835494
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+580C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835494 | ||||||
chr10:50835805
|
CTCTT | C | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+265_604+268del others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835805 | ||||||
chr10:50835884
|
T | A | 1 | a0001c0002t0004g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.604+190A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835884 | ||||||
chr10:50835886
|
A | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+188T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835886 | ||||||
chr10:50835970
|
A | G | 3 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0224 | 3 | HG02132.hp1 NA19079.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.604+104T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835970 | ||||||
chr10:50835988
|
CA | C | 19 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.604+85delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835988 | ||||||
chr10:50836380
|
G | C | 9 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-68C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836380 | ||||||
chr10:50836539
|
T | A | 1 | a0001c0001t0017g0266 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.366-227A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836539 | ||||||
chr10:50836590
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.366-278C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836590 | ||||||
chr10:50836721
|
A | G | 1 | a0001c0001t0016g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.366-409T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836721 | ||||||
chr10:50836795
|
T | C | 46 | a0001c0001t0001g0225a0001c0001t0001g0276a0001c0001t0003g0018others(43): Show | 55 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.366-483A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836795 | ||||||
chr10:50837015
|
T | C | 1 | a0001c0001t0007g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.366-703A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837015 | ||||||
chr10:50837021
|
C | T | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.366-709G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837021 | ||||||
chr10:50837297
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.366-985G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837297 | ||||||
chr10:50837406
|
T | C | 1 | a0001c0001t0005g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.366-1094A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837406 | ||||||
chr10:50837415
|
C | T | 4 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1103G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837415 | ||||||
chr10:50837475
|
C | A | 9 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-1163G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837475 | ||||||
chr10:50837567
|
T | A | 4 | a0001c0002t0004g0254a0001c0002t0004g0256a0001c0009t0004g0255others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1255A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837567 | ||||||
chr10:50837656
|
C | T | 1 | a0001c0001t0008g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.366-1344G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837656 | ||||||
chr10:50837831
|
T | C | 2 | a0001c0001t0011g0092a0001c0001t0011g0093 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.366-1519A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837831 | ||||||
chr10:50837871
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.366-1559G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837871 | ||||||
chr10:50837894
|
A | T | 2 | a0001c0002t0004g0071a0001c0002t0004g0077 | 2 | NA18977.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.366-1582T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837894 | ||||||
chr10:50837917
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.366-1605T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837917 | ||||||
chr10:50838036
|
A | G | 7 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.366-1724T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838036 | ||||||
chr10:50838044
|
C | T | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1732G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838044 | ||||||
chr10:50838206
|
G | A | 4 | a0001c0003t0001g0025a0001c0003t0001g0156a0001c0003t0007g0231others(1): Show | 5 | HG00280.hp2 NA18948.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-1894C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838206 | ||||||
chr10:50838272
|
G | A | 2 | a0001c0001t0005g0272a0001c0001t0005g0273 | 2 | HG02602.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-1960C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838272 | ||||||
chr10:50838344
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.366-2032C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838344 | ||||||
chr10:50838625
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.366-2313G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838625 | ||||||
chr10:50838664
|
T | C | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-2352A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838664 | ||||||
chr10:50839156
|
C | A | 3 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017 | 6 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+2706G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839156 | ||||||
chr10:50839256
|
C | T | 1 | a0001c0008t0001g0039 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.365+2606G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839256 | ||||||
chr10:50839525
|
G | A | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.365+2337C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839525 | ||||||
chr10:50839787
|
G | A | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+2075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839787 | ||||||
chr10:50839852
|
A | G | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.365+2010T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839852 | ||||||
chr10:50839991
|
C | T | 2 | a0001c0001t0010g0031a0001c0001t0010g0097 | 3 | HG01192.hp1 HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.365+1871G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839991 | ||||||
chr10:50840004
|
A | C | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.365+1858T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840004 | ||||||
chr10:50840035
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(277): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.365+1827A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840035 | ||||||
chr10:50840196
|
A | G | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.365+1666T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840196 | ||||||
chr10:50840217
|
G | A | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+1645C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840217 | ||||||
chr10:50840240
|
A | C | 1 | a0001c0001t0002g0190 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.365+1622T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840240 | ||||||
chr10:50840276
|
A | AT | 100 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(97): Show | 114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.365+1585dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840276 | ||||||
chr10:50840299
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.365+1563G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840299 | ||||||
chr10:50840710
|
A | G | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+1152T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840710 | ||||||
chr10:50840848
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.365+1014C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840848 | ||||||
chr10:50841028
|
A | G | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.365+834T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841028 | ||||||
chr10:50841173
|
A | G | 1 | a0001c0001t0003g0287 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.365+689T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841173 | ||||||
chr10:50841318
|
C | T | 6 | a0001c0001t0037g0050a0001c0008t0001g0039a0001c0008t0017g0042others(3): Show | 6 | HG02451.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+544G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841318 | ||||||
chr10:50841477
|
G | A | 1 | a0002c0004t0044g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.365+385C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841477 | ||||||
chr10:50842074
|
A | AAC | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-84_235-83dupGT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842074 | ||||||
chr10:50842140
|
A | G | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.235-148T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842140 | ||||||
chr10:50842153
|
T | G | 1 | a0001c0003t0001g0230 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.235-161A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842153 | ||||||
chr10:50842303
|
T | C | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235-311A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842303 | ||||||
chr10:50842472
|
G | A | 1 | a0001c0002t0004g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235-480C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842472 | ||||||
chr10:50842476
|
T | C | 1 | a0001c0001t0039g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-484A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842476 | ||||||
chr10:50842700
|
C | G | 1 | a0001c0001t0015g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.235-708G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842700 | ||||||
chr10:50843053
|
G | A | 1 | a0001c0001t0003g0150 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.234+935C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843053 | ||||||
chr10:50843367
|
T | A | 12 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+621A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843367 | ||||||
chr10:50843482
|
T | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(124): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.234+506A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843482 | ||||||
chr10:50843899
|
C | T | 31 | a0001c0001t0003g0018a0001c0001t0003g0263a0001c0001t0003g0270others(28): Show | 39 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.234+89G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843899 | ||||||
chr10:50844185
|
C | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-63G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844185 | ||||||
chr10:50844362
|
AAT | A | 12 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-242_100-241del others(2): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844362 | ||||||
chr10:50844563
|
A | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(281): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.100-441T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844563 | ||||||
chr10:50844708
|
A | G | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-586T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844708 | ||||||
chr10:50844719
|
C | T | 18 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(15): Show | 25 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-597G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844719 | ||||||
chr10:50844749
|
G | A | 1 | a0001c0002t0004g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100-627C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844749 | ||||||
chr10:50844839
|
T | C | 1 | a0001c0001t0005g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-717A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844839 | ||||||
chr10:50845326
|
C | A | 12 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-1204G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845326 | ||||||
chr10:50845559
|
AT | A | 12 | a0001c0002t0004g0002a0001c0002t0004g0069a0001c0002t0004g0070others(9): Show | 16 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-1438delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845559 | ||||||
chr10:50845911
|
G | A | 3 | a0001c0001t0002g0051a0001c0001t0002g0151a0001c0001t0002g0161 | 3 | HG00673.hp1 NA18947.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.100-1789C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845911 | ||||||
chr10:50845953
|
C | CA | 87 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.100-1832dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845953 | ||||||
chr10:50845953
|
CA | C | 8 | a0001c0001t0002g0190a0001c0001t0008g0006a0001c0001t0008g0098others(5): Show | 10 | HG02135.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-1832delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845953 | ||||||
chr10:50846046
|
C | T | 1 | a0001c0001t0023g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.100-1924G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846046 | ||||||
chr10:50846097
|
C | A | 15 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(12): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-1975G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846097 | ||||||
chr10:50846137
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.100-2015T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846137 | ||||||
chr10:50846214
|
C | A | 1 | a0002c0004t0044g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-2092G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846214 | ||||||
chr10:50846384
|
A | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2262T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846384 | ||||||
chr10:50846495
|
C | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-2373G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846495 | ||||||
chr10:50846526
|
A | G | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.100-2404T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846526 | ||||||
chr10:50846606
|
A | G | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2484T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846606 | ||||||
chr10:50846728
|
A | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(82): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.100-2606T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846728 | ||||||
chr10:50846821
|
T | A | 1 | a0001c0001t0043g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-2699A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846821 | ||||||
chr10:50846916
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-2794C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846916 | ||||||
chr10:50847261
|
G | A | 1 | a0002c0004t0044g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-3139C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847261 | ||||||
chr10:50847479
|
A | T | 1 | a0001c0001t0015g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100-3357T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847479 | ||||||
chr10:50847743
|
C | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-3621G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847743 | ||||||
chr10:50847872
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-3750C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847872 | ||||||
chr10:50847965
|
C | A | 4 | a0001c0002t0004g0254a0001c0002t0004g0256a0001c0009t0004g0255others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3843G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847965 | ||||||
chr10:50848012
|
C | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-3890G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848012 | ||||||
chr10:50848145
|
A | T | 2 | a0001c0002t0004g0086a0001c0002t0013g0085 | 2 | HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.100-4023T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848145 | ||||||
chr10:50848354
|
C | G | 1 | a0001c0001t0003g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100-4232G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848354 | ||||||
chr10:50848520
|
A | C | 1 | a0001c0002t0004g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100-4398T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848520 | ||||||
chr10:50848642
|
A | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-4520T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848642 | ||||||
chr10:50848851
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0002g0165 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.100-4729C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848851 | ||||||
chr10:50848897
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(123): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.100-4775T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848897 | ||||||
chr10:50849010
|
G | T | 2 | a0001c0001t0011g0092a0001c0001t0011g0093 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.100-4888C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849010 | ||||||
chr10:50849085
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-4963A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849085 | ||||||
chr10:50849142
|
A | G | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-5020T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849142 | ||||||
chr10:50849195
|
A | G | 3 | a0001c0005t0001g0207a0001c0005t0024g0208a0001c0005t0048g0209 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.100-5073T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849195 | ||||||
chr10:50849208
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-5086C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849208 | ||||||
chr10:50849248
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0169others(79): Show | 103 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.100-5126A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849248 | ||||||
chr10:50849253
|
A | G | 1 | a0001c0001t0002g0007 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.100-5131T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849253 | ||||||
chr10:50849370
|
C | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-5248G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849370 | ||||||
chr10:50849438
|
G | A | 12 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-5316C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849438 | ||||||
chr10:50849559
|
A | G | 12 | a0001c0002t0004g0002a0001c0002t0004g0069a0001c0002t0004g0070others(9): Show | 16 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-5437T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849559 | ||||||
chr10:50849740
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-5618C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849740 | ||||||
chr10:50849786
|
C | CT | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(166): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.100-5665dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849786 | ||||||
chr10:50849786
|
C | CTT | 22 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(19): Show | 22 | HG00544.hp2 HG01123.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-5666_100-5665d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849786 | ||||||
chr10:50849889
|
C | G | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-5767G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849889 | ||||||
chr10:50849938
|
C | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-5816G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849938 | ||||||
chr10:50849962
|
T | G | 1 | a0001c0001t0002g0157 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.100-5840A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849962 | ||||||
chr10:50850004
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.100-5882G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850004 | ||||||
chr10:50850154
|
G | A | 19 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(16): Show | 26 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-6032C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850154 | ||||||
chr10:50850217
|
T | C | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0049g0167 | 3 | HG00438.hp2 HG00558.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.100-6095A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850217 | ||||||
chr10:50850578
|
A | G | 1 | a0001c0001t0005g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100-6456T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850578 | ||||||
chr10:50850592
|
T | TTG | 60 | a0001c0001t0001g0276a0001c0001t0003g0018a0001c0001t0003g0033others(57): Show | 72 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.100-6472_100-6471d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850592 | ||||||
chr10:50850978
|
G | T | 5 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6856C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850978 | ||||||
chr10:50851005
|
C | G | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-6883G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851005 | ||||||
chr10:50851327
|
A | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-7205T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851327 | ||||||
chr10:50851610
|
GTC | G | 12 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-7490_100-7489d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851610 | ||||||
chr10:50851658
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-7536C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851658 | ||||||
chr10:50851956
|
T | C | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100-7834A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851956 | ||||||
chr10:50852185
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+7657G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852185 | ||||||
chr10:50852341
|
G | A | 44 | a0001c0001t0001g0276a0001c0001t0003g0018a0001c0001t0003g0033others(41): Show | 53 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+7501C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852341 | ||||||
chr10:50852453
|
T | C | 1 | a0001c0008t0017g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+7389A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852453 | ||||||
chr10:50852576
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0197 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.99+7266G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852576 | ||||||
chr10:50852761
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.99+7081T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852761 | ||||||
chr10:50852869
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+6973G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852869 | ||||||
chr10:50852882
|
C | T | 1 | a0001c0002t0004g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+6960G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852882 | ||||||
chr10:50852902
|
C | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0169others(77): Show | 101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+6940G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852902 | ||||||
chr10:50852950
|
C | T | 2 | a0001c0001t0028g0052a0002c0004t0045g0200 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.99+6892G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852950 | ||||||
chr10:50853040
|
G | A | 1 | a0001c0001t0039g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+6802C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853040 | ||||||
chr10:50853042
|
G | A | 5 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+6800C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853042 | ||||||
chr10:50853091
|
G | C | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+6751C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853091 | ||||||
chr10:50853133
|
G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6709C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853133 | ||||||
chr10:50853187
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.99+6655A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853187 | ||||||
chr10:50853275
|
C | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(281): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.99+6567G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853275 | ||||||
chr10:50853382
|
A | G | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+6460T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853382 | ||||||
chr10:50853465
|
G | A | 1 | a0001c0012t0034g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+6377C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853465 | ||||||
chr10:50853750
|
AT | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(159): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.99+6091delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853750 | ||||||
chr10:50853750
|
ATT | A | 18 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0061others(15): Show | 19 | HG00423.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+6090_99+6091del others(2): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853750 | ||||||
chr10:50853773
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+6069C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853773 | ||||||
chr10:50853797
|
T | A | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+6045A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853797 | ||||||
chr10:50853801
|
T | C | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+6041A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853801 | ||||||
chr10:50853803
|
T | TA | 11 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+6038dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853803 | ||||||
chr10:50853804
|
A | T | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(252): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.99+6038T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853804 | ||||||
chr10:50853805
|
A | T | 1 | a0001c0001t0023g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.99+6037T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853805 | ||||||
chr10:50853823
|
TA | T | 45 | a0001c0001t0001g0276a0001c0001t0003g0018a0001c0001t0003g0033others(42): Show | 54 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.99+6018delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853823 | ||||||
chr10:50853891
|
A | T | 1 | a0001c0002t0004g0072 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99+5951T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853891 | ||||||
chr10:50854115
|
T | C | 3 | a0001c0001t0005g0251a0001c0001t0005g0253a0001c0001t0014g0252 | 3 | HG01109.hp2 HG01167.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.99+5727A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854115 | ||||||
chr10:50854200
|
A | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0194 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.99+5642T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854200 | ||||||
chr10:50854429
|
A | G | 7 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0280others(4): Show | 7 | HG02280.hp1 HG03654.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+5413T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854429 | ||||||
chr10:50854998
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+4844G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854998 | ||||||
chr10:50855053
|
T | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+4789A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855053 | ||||||
chr10:50855095
|
T | C | 1 | a0001c0001t0003g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.99+4747A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855095 | ||||||
chr10:50855245
|
G | C | 2 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.99+4597C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855245 | ||||||
chr10:50855262
|
T | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(56): Show | 73 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.99+4580A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855262 | ||||||
chr10:50855288
|
A | C | 1 | a0002c0006t0006g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+4554T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855288 | ||||||
chr10:50855360
|
A | T | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.99+4482T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855360 | ||||||
chr10:50855361
|
T | G | 1 | a0002c0006t0006g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+4481A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855361 | ||||||
chr10:50855385
|
T | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+4457A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855385 | ||||||
chr10:50855510
|
C | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0169others(78): Show | 102 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+4332G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855510 | ||||||
chr10:50855671
|
C | A | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.99+4171G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855671 | ||||||
chr10:50855911
|
C | G | 15 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(12): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+3931G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855911 | ||||||
chr10:50856273
|
G | A | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.99+3569C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856273 | ||||||
chr10:50856287
|
A | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0169others(79): Show | 103 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.99+3555T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856287 | ||||||
chr10:50856307
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+3535G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856307 | ||||||
chr10:50856463
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.99+3379G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856463 | ||||||
chr10:50856509
|
G | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(111): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.99+3333C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856509 | ||||||
chr10:50856558
|
T | C | 1 | a0001c0002t0004g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+3284A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856558 | ||||||
chr10:50856582
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.99+3260T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856582 | ||||||
chr10:50856722
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+3120C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856722 | ||||||
chr10:50856800
|
TGTG | T | 1 | a0001c0001t0005g0010 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99+3039_99+3041del others(3): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856800 | ||||||
chr10:50856823
|
G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+3019C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856823 | ||||||
chr10:50856951
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.99+2891G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856951 | ||||||
chr10:50856976
|
C | T | 1 | a0001c0008t0001g0039 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.99+2866G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856976 | ||||||
chr10:50857083
|
T | C | 1 | a0001c0001t0005g0143 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.99+2759A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857083 | ||||||
chr10:50857162
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0005g0277a0001c0001t0005g0278others(5): Show | 9 | HG02280.hp1 HG03654.hp1 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2680G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857162 | ||||||
chr10:50857187
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+2655G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857187 | ||||||
chr10:50857237
|
G | A | 2 | a0001c0002t0004g0087a0001c0012t0034g0154 | 2 | HG03225.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.99+2605C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857237 | ||||||
chr10:50857646
|
C | G | 1 | a0001c0001t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.99+2196G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857646 | ||||||
chr10:50857778
|
T | C | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+2064A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857778 | ||||||
chr10:50857815
|
G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+2027C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857815 | ||||||
chr10:50857975
|
A | T | 1 | a0001c0001t0005g0010 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99+1867T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857975 | ||||||
chr10:50857985
|
C | T | 1 | a0001c0001t0003g0286 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.99+1857G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857985 | ||||||
chr10:50858310
|
TG | T | 22 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(19): Show | 25 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.99+1531delC | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858310 | ||||||
chr10:50858603
|
G | C | 1 | a0001c0001t0012g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+1239C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858603 | ||||||
chr10:50858615
|
T | C | 1 | a0001c0002t0004g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+1227A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858615 | ||||||
chr10:50858935
|
G | A | 2 | a0001c0002t0004g0019a0001c0002t0004g0105 | 3 | HG00621.hp1 NA19011.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.99+907C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858935 | ||||||
chr10:50859031
|
G | T | 1 | a0001c0001t0005g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.99+811C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859031 | ||||||
chr10:50859037
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+805G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859037 | ||||||
chr10:50859049
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.99+793A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859049 | ||||||
chr10:50859268
|
A | G | 2 | a0001c0001t0028g0052a0002c0004t0045g0200 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.99+574T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859268 | ||||||
chr10:50859414
|
C | T | 1 | a0001c0001t0005g0265 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+428G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859414 | ||||||
chr10:50859464
|
G | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+378C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859464 | ||||||
chr10:50859527
|
C | T | 1 | a0001c0005t0001g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+315G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859527 | ||||||
chr10:50859675
|
T | C | 1 | a0001c0001t0005g0271 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+167A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859675 | ||||||
chr10:50859814
|
A | G | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+28T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859814 | ||||||
chr10:50860152
|
A | G | 1 | a0001c0001t0021g0110 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-45-167T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860152 | ||||||
chr10:50860192
|
C | CA | 16 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0261others(13): Show | 17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-45-208dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860192 | ||||||
chr10:50860196
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-45-211T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860196 | ||||||
chr10:50860449
|
G | C | 1 | a0001c0001t0002g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-45-464C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860449 | ||||||
chr10:50860683
|
G | A | 1 | a0001c0001t0005g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-45-698C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860683 | ||||||
chr10:50860705
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(265): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.-45-720C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860705 | ||||||
chr10:50860930
|
T | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-45-945A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860930 | ||||||
chr10:50861038
|
T | C | 3 | a0001c0005t0001g0207a0001c0005t0024g0208a0001c0005t0048g0209 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-45-1053A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861038 | ||||||
chr10:50861051
|
G | C | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-45-1066C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861051 | ||||||
chr10:50861060
|
G | A | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-45-1075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861060 | ||||||
chr10:50861440
|
A | G | 1 | a0001c0002t0004g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-45-1455T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861440 | ||||||
chr10:50861502
|
G | C | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-45-1517C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861502 | ||||||
chr10:50861513
|
T | C | 1 | a0001c0001t0019g0242 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-45-1528A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861513 | ||||||
chr10:50861771
|
A | G | 1 | a0001c0001t0023g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-45-1786T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861771 | ||||||
chr10:50861784
|
A | G | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-45-1799T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861784 | ||||||
chr10:50861804
|
T | C | 2 | a0001c0001t0016g0041a0001c0001t0039g0038 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-45-1819A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861804 | ||||||
chr10:50861856
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-45-1871T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861856 | ||||||
chr10:50861947
|
C | T | 1 | a0001c0001t0005g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-45-1962G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861947 | ||||||
chr10:50861992
|
G | C | 30 | a0001c0001t0003g0018a0001c0001t0003g0263a0001c0001t0003g0270others(27): Show | 38 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.-45-2007C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861992 | ||||||
chr10:50862163
|
C | T | 1 | a0003c0010t0001g0136 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-46+1870G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50862163 | ||||||
chr10:50862974
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-46+1059G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50862974 | ||||||
chr10:50863043
|
G | T | 2 | a0001c0001t0005g0277a0001c0001t0049g0167 | 2 | NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-46+990C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863043 | ||||||
chr10:50863116
|
T | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-46+917A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863116 | ||||||
chr10:50863128
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-46+905G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863128 | ||||||
chr10:50863269
|
C | T | 4 | a0001c0001t0021g0110a0001c0005t0001g0207a0001c0005t0024g0208others(1): Show | 4 | HG01257.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+764G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863269 | ||||||
chr10:50863319
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0099 | 3 | NA18947.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-46+714C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863319 | ||||||
chr10:50863417
|
A | G | 1 | a0001c0001t0001g0020 | 2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-46+616T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863417 | ||||||
chr10:50863484
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-46+549T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863484 | ||||||
chr10:50863567
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-46+466C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863567 | ||||||
chr10:50863633
|
G | T | 1 | a0001c0003t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-46+400C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863633 | ||||||
chr10:50863653
|
A | T | 1 | a0002c0004t0018g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-46+380T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863653 | ||||||
chr10:50863673
|
A | G | 14 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(11): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-46+360T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863673 | ||||||
chr10:50863733
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-46+300C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863733 | ||||||
chr10:50863774
|
A | G | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+259T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863774 | ||||||
chr10:50863825
|
T | A | 20 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46+208A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863825 | ||||||
chr10:50863826
|
A | C | 20 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46+207T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863826 | ||||||
chr10:50863902
|
G | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-46+131C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863902 | ||||||
chr10:50864082
|
T | C | 1 | a0002c0006t0006g0046 | 1 | HG02451.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.-93-2A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864082 | ||||||
chr10:50864159
|
C | T | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-79G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864159 | ||||||
chr10:50864199
|
A | C | 4 | a0001c0001t0001g0113a0001c0001t0020g0112a0001c0002t0004g0019others(1): Show | 5 | HG00621.hp1 NA19002.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-119T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864199 | ||||||
chr10:50864429
|
T | C | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-349A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864429 | ||||||
chr10:50864441
|
G | C | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-361C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864441 | ||||||
chr10:50864535
|
A | G | 1 | a0001c0001t0005g0264 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-93-455T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864535 | ||||||
chr10:50864542
|
G | GT | 93 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(90): Show | 107 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-93-463dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864542 | ||||||
chr10:50864618
|
T | C | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-538A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864618 | ||||||
chr10:50864620
|
T | C | 1 | a0001c0001t0043g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-93-540A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864620 | ||||||
chr10:50864679
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-599G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864679 | ||||||
chr10:50864690
|
C | T | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-93-610G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864690 | ||||||
chr10:50864721
|
C | T | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-641G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864721 | ||||||
chr10:50864744
|
G | A | 1 | a0001c0001t0003g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-93-664C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864744 | ||||||
chr10:50864826
|
C | T | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-93-746G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864826 | ||||||
chr10:50864907
|
C | T | 2 | a0001c0001t0005g0280a0001c0001t0005g0281 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-93-827G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864907 | ||||||
chr10:50864908
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02083.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-93-828C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864908 | ||||||
chr10:50864919
|
A | G | 1 | a0001c0001t0003g0018 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-93-839T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864919 | ||||||
chr10:50865223
|
C | A | 3 | a0001c0001t0005g0251a0001c0001t0005g0253a0001c0001t0014g0252 | 3 | HG01109.hp2 HG01167.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-93-1143G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865223 | ||||||
chr10:50865232
|
C | CTGGG | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-1156_-93-1153d others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865232 | ||||||
chr10:50865250
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-93-1170G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865250 | ||||||
chr10:50865296
|
T | TTAC | 20 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-93-1219_-93-1217d others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865296 | ||||||
chr10:50865296
|
TTAC | T | 19 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93-1219_-93-1217d others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865296 | ||||||
chr10:50865302
|
C | G | 2 | a0001c0001t0028g0052a0002c0004t0045g0200 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-93-1222G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865302 | ||||||
chr10:50865388
|
G | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93-1308C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865388 | ||||||
chr10:50865421
|
A | T | 1 | a0001c0001t0010g0031 | 2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-93-1341T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865421 | ||||||
chr10:50865510
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(57): Show | 74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-93-1430T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865510 | ||||||
chr10:50865603
|
T | C | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-1523A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865603 | ||||||
chr10:50865733
|
G | T | 2 | a0001c0001t0001g0111a0001c0001t0003g0016 | 3 | HG00280.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-93-1653C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865733 | ||||||
chr10:50865853
|
C | T | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-1773G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865853 | ||||||
chr10:50866011
|
A | G | 1 | a0001c0001t0040g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-93-1931T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866011 | ||||||
chr10:50866013
|
A | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-1933T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866013 | ||||||
chr10:50866042
|
G | C | 1 | a0001c0002t0004g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-93-1962C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866042 | ||||||
chr10:50866079
|
T | C | 20 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(17): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93-1999A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866079 | ||||||
chr10:50866087
|
C | T | 31 | a0001c0001t0001g0074a0001c0001t0005g0251a0001c0001t0005g0253others(28): Show | 35 | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-93-2007G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866087 | ||||||
chr10:50866760
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-2680C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866760 | ||||||
chr10:50866760
|
G | T | 1 | a0001c0001t0003g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-93-2680C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866760 | ||||||
chr10:50866908
|
G | A | 1 | a0001c0008t0017g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-93-2828C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866908 | ||||||
chr10:50867016
|
GT | G | 16 | a0001c0001t0003g0286a0001c0001t0008g0006a0001c0001t0008g0098others(13): Show | 19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-93-2937delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867016 | ||||||
chr10:50867151
|
C | T | 1 | a0001c0002t0013g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-93-3071G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867151 | ||||||
chr10:50867204
|
A | C | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-93-3124T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867204 | ||||||
chr10:50867270
|
T | C | 1 | a0001c0002t0004g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-93-3190A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867270 | ||||||
chr10:50867321
|
G | A | 3 | a0001c0005t0001g0207a0001c0005t0024g0208a0001c0005t0048g0209 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-93-3241C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867321 | ||||||
chr10:50867464
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-93-3384A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867464 | ||||||
chr10:50867685
|
A | G | 1 | a0001c0001t0010g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-93-3605T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867685 | ||||||
chr10:50867765
|
A | G | 1 | a0001c0001t0003g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-93-3685T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867765 | ||||||
chr10:50867786
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-93-3706C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867786 | ||||||
chr10:50867812
|
G | T | 20 | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-93-3732C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867812 | ||||||
chr10:50867841
|
A | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-3761T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867841 | ||||||
chr10:50867901
|
C | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-3821G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867901 | ||||||
chr10:50868038
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-3958C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868038 | ||||||
chr10:50868144
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0027g0084 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-93-4064A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868144 | ||||||
chr10:50868186
|
T | G | 1 | a0001c0001t0002g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-93-4106A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868186 | ||||||
chr10:50868192
|
C | T | 1 | a0001c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-93-4112G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868192 | ||||||
chr10:50868222
|
A | G | 1 | a0001c0001t0043g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-93-4142T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868222 | ||||||
chr10:50868506
|
A | C | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.-93-4426T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868506 | ||||||
chr10:50868801
|
A | T | 19 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93-4721T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868801 | ||||||
chr10:50868973
|
T | C | 1 | a0001c0001t0003g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-93-4893A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868973 | ||||||
chr10:50869312
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-5232C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50869312 | ||||||
chr10:50869441
|
G | A | 1 | a0001c0001t0007g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-93-5361C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50869441 | ||||||
chr10:50869812
|
C | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(59): Show | 76 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-93-5732G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50869812 | ||||||
chr10:50870098
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-93-6018G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870098 | ||||||
chr10:50870379
|
G | A | 4 | a0001c0002t0004g0254a0001c0002t0004g0256a0001c0009t0004g0255others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-6299C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870379 | ||||||
chr10:50870425
|
G | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(103): Show | 129 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-93-6345C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870425 | ||||||
chr10:50870499
|
A | C | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-6419T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870499 | ||||||
chr10:50870665
|
G | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(104): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-93-6585C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870665 | ||||||
chr10:50870822
|
C | A | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-93-6742G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870822 | ||||||
chr10:50870902
|
G | C | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 21 | HG00673.hp2 HG02135.hp1 HG02148.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93-6822C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870902 | ||||||
chr10:50870968
|
T | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(277): Show | 331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.-93-6888A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870968 | ||||||
chr10:50871130
|
A | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-7050T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871130 | ||||||
chr10:50871325
|
C | A | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-93-7245G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871325 | ||||||
chr10:50871326
|
G | A | 3 | a0001c0001t0028g0052a0001c0002t0013g0088a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-93-7246C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871326 | ||||||
chr10:50871503
|
T | C | 1 | a0001c0001t0005g0010 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-7423A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871503 | ||||||
chr10:50871569
|
G | C | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-7489C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871569 | ||||||
chr10:50871805
|
T | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-7725A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871805 | ||||||
chr10:50871816
|
C | T | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-7736G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871816 | ||||||
chr10:50871981
|
A | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(281): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-93-7901T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871981 | ||||||
chr10:50872020
|
ATAT | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0099 | 3 | NA18947.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-93-7943_-93-7941d others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872020 | ||||||
chr10:50872023
|
T | C | 12 | a0001c0001t0001g0029a0001c0001t0001g0203a0001c0001t0001g0204others(9): Show | 13 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-7943A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872023 | ||||||
chr10:50872128
|
C | CTT | 17 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.-93-8049_-93-8048i others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872128 | ||||||
chr10:50872220
|
A | G | 1 | a0001c0002t0004g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-93-8140T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872220 | ||||||
chr10:50872353
|
A | G | 1 | a0001c0001t0005g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-93-8273T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872353 | ||||||
chr10:50872525
|
G | A | 1 | a0001c0001t0003g0287 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-93-8445C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872525 | ||||||
chr10:50872668
|
G | A | 3 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-8588C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872668 | ||||||
chr10:50872779
|
C | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-8699G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872779 | ||||||
chr10:50872828
|
T | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-8748A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872828 | ||||||
chr10:50872898
|
A | C | 1 | a0001c0001t0021g0110 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-93-8818T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872898 | ||||||
chr10:50872905
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-93-8825C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872905 | ||||||
chr10:50872946
|
C | CT | 56 | a0001c0001t0001g0011a0001c0001t0001g0091a0001c0001t0001g0103others(53): Show | 66 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-93-8867dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | ||||||
chr10:50872946
|
C | CTT | 8 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0161others(5): Show | 9 | HG00140.hp1 HG00558.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93-8868_-93-8867d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | ||||||
chr10:50872946
|
CT | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0099others(86): Show | 110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-93-8867delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | ||||||
chr10:50872946
|
CTT | C | 10 | a0001c0001t0001g0197a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 12 | HG00621.hp2 HG00639.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93-8868_-93-8867d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | ||||||
chr10:50872946
|
CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(4): Show | 10 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-8877_-93-8867d others(13): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | ||||||
chr10:50872946
|
CTTTTTTT others(7): Show |
C | 14 | a0001c0001t0001g0276a0001c0001t0003g0033a0001c0001t0003g0259others(11): Show | 15 | HG00438.hp1 HG01516.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.-93-8880_-93-8867d others(16): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | ||||||
chr10:50872986
|
C | T | 1 | a0001c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-93-8906G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872986 | ||||||
chr10:50872987
|
G | A | 2 | a0001c0001t0037g0050a0002c0004t0044g0049 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-8907C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872987 | ||||||
chr10:50872997
|
C | G | 2 | a0001c0001t0028g0052a0002c0004t0045g0200 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-93-8917G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872997 | ||||||
chr10:50873231
|
T | C | 8 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(5): Show | 11 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-93-9151A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873231 | ||||||
chr10:50873248
|
G | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(241): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-93-9168C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873248 | ||||||
chr10:50873290
|
A | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-9210T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873290 | ||||||
chr10:50873538
|
A | G | 1 | a0001c0001t0003g0018 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-93-9458T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873538 | ||||||
chr10:50873575
|
A | G | 17 | a0001c0001t0001g0029a0001c0001t0001g0203a0001c0001t0001g0204others(14): Show | 18 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-93-9495T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873575 | ||||||
chr10:50873585
|
A | T | 1 | a0002c0004t0045g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-93-9505T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873585 | ||||||
chr10:50873699
|
C | T | 101 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0063others(98): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-93-9619G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873699 | ||||||
chr10:50873801
|
G | C | 3 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017 | 6 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93-9721C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873801 | ||||||
chr10:50873960
|
T | C | 1 | a0001c0003t0001g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-93-9880A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873960 | ||||||
chr10:50874158
|
G | A | 2 | a0001c0002t0004g0086a0001c0002t0013g0085 | 2 | HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-93-10078C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874158 | ||||||
chr10:50874204
|
G | A | 1 | a0001c0001t0007g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-93-10124C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874204 | ||||||
chr10:50874223
|
T | C | 1 | a0002c0004t0006g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-93-10143A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874223 | ||||||
chr10:50874265
|
A | G | 1 | a0001c0001t0002g0157 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-93-10185T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874265 | ||||||
chr10:50874290
|
TA | T | 40 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(37): Show | 48 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-93-10211delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874290 | ||||||
chr10:50874845
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-94+10736G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874845 | ||||||
chr10:50874893
|
T | C | 2 | a0001c0001t0037g0050a0002c0004t0044g0049 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+10688A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874893 | ||||||
chr10:50874948
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+10633C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874948 | ||||||
chr10:50875061
|
G | A | 36 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(33): Show | 43 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-94+10520C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875061 | ||||||
chr10:50875141
|
T | C | 1 | a0001c0003t0001g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-94+10440A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875141 | ||||||
chr10:50875285
|
T | TA | 36 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(33): Show | 43 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-94+10295dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875285 | ||||||
chr10:50875343
|
A | T | 4 | a0001c0003t0001g0025a0001c0003t0001g0156a0001c0003t0007g0231others(1): Show | 5 | HG00280.hp2 NA18948.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94+10238T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875343 | ||||||
chr10:50875411
|
C | T | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-94+10170G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875411 | ||||||
chr10:50875419
|
G | A | 3 | a0001c0012t0034g0154a0002c0004t0018g0034a0002c0004t0018g0153 | 3 | HG02886.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-94+10162C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875419 | ||||||
chr10:50875480
|
A | G | 23 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(20): Show | 30 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-94+10101T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875480 | ||||||
chr10:50875667
|
T | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+9914A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875667 | ||||||
chr10:50875961
|
T | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+9620A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875961 | ||||||
chr10:50876194
|
G | A | 11 | a0001c0001t0005g0043a0001c0001t0011g0092a0001c0001t0011g0093others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-94+9387C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876194 | ||||||
chr10:50876593
|
T | C | 1 | a0001c0003t0001g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-94+8988A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876593 | ||||||
chr10:50876598
|
G | A | 1 | a0001c0001t0030g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-94+8983C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876598 | ||||||
chr10:50876648
|
C | T | 1 | a0001c0001t0035g0155 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-94+8933G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876648 | ||||||
chr10:50876658
|
C | A | 1 | a0001c0001t0015g0096 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-94+8923G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876658 | ||||||
chr10:50876742
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-94+8839G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876742 | ||||||
chr10:50876769
|
T | C | 9 | a0001c0001t0003g0033a0001c0001t0003g0259a0001c0001t0003g0260others(6): Show | 10 | HG02523.hp1 HG02602.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+8812A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876769 | ||||||
chr10:50876846
|
TAC | T | 3 | a0001c0012t0034g0154a0002c0004t0018g0034a0002c0004t0018g0153 | 3 | HG02886.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-94+8733_-94+8734d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876846 | ||||||
chr10:50876904
|
C | T | 6 | a0001c0001t0005g0043a0001c0008t0001g0039a0001c0008t0017g0042others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94+8677G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876904 | ||||||
chr10:50877267
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-94+8314G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877267 | ||||||
chr10:50877334
|
A | G | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-94+8247T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877334 | ||||||
chr10:50877531
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-94+8050T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877531 | ||||||
chr10:50877536
|
C | T | 2 | a0001c0001t0011g0092a0001c0001t0011g0093 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+8045G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877536 | ||||||
chr10:50877615
|
T | C | 1 | a0001c0003t0001g0230 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-94+7966A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877615 | ||||||
chr10:50877796
|
T | C | 5 | a0001c0001t0005g0043a0001c0008t0001g0039a0002c0006t0006g0044others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94+7785A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877796 | ||||||
chr10:50877848
|
C | T | 13 | a0001c0001t0005g0043a0001c0001t0011g0092a0001c0001t0011g0093others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+7733G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877848 | ||||||
chr10:50877849
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-94+7732C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877849 | ||||||
chr10:50877989
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-94+7592C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877989 | ||||||
chr10:50878017
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0246 | 3 | NA19066.hp1 NA19081.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-94+7564C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878017 | ||||||
chr10:50878063
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG00738.hp2 HG01081.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+7518T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878063 | ||||||
chr10:50878098
|
G | A | 2 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-94+7483C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878098 | ||||||
chr10:50878165
|
A | G | 46 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(43): Show | 58 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-94+7416T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878165 | ||||||
chr10:50878350
|
G | T | 13 | a0001c0001t0005g0043a0001c0001t0011g0092a0001c0001t0011g0093others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+7231C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878350 | ||||||
chr10:50878567
|
G | C | 1 | a0001c0001t0037g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-94+7014C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878567 | ||||||
chr10:50878603
|
T | G | 2 | a0001c0003t0007g0231a0001c0003t0007g0232 | 2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-94+6978A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878603 | ||||||
chr10:50878667
|
C | T | 2 | a0001c0001t0002g0051a0001c0001t0002g0151 | 2 | NA18947.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-94+6914G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878667 | ||||||
chr10:50878695
|
T | A | 13 | a0001c0001t0005g0043a0001c0001t0011g0092a0001c0001t0011g0093others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+6886A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878695 | ||||||
chr10:50878709
|
C | T | 1 | a0001c0001t0003g0150 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-94+6872G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878709 | ||||||
chr10:50878918
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-94+6663G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878918 | ||||||
chr10:50879098
|
G | A | 2 | a0001c0001t0037g0050a0002c0004t0044g0049 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+6483C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879098 | ||||||
chr10:50879173
|
T | G | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(236): Show | 281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.-94+6408A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879173 | ||||||
chr10:50879236
|
T | C | 2 | a0001c0002t0004g0087a0001c0002t0013g0088 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-94+6345A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879236 | ||||||
chr10:50879400
|
G | T | 1 | a0001c0002t0004g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-94+6181C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879400 | ||||||
chr10:50879586
|
C | T | 1 | a0001c0001t0005g0264 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-94+5995G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879586 | ||||||
chr10:50879897
|
G | C | 48 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(45): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-94+5684C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879897 | ||||||
chr10:50880116
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(283): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.-94+5465G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880116 | ||||||
chr10:50880499
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-94+5082G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880499 | ||||||
chr10:50880521
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-94+5060C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880521 | ||||||
chr10:50880633
|
G | T | 5 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0010g0097others(2): Show | 7 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+4948C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880633 | ||||||
chr10:50880857
|
G | A | 1 | a0001c0001t0005g0010 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+4724C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880857 | ||||||
chr10:50881029
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 11 | HG00738.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-94+4552C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881029 | ||||||
chr10:50881077
|
C | A | 1 | a0001c0001t0002g0238 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-94+4504G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881077 | ||||||
chr10:50881084
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-94+4497C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881084 | ||||||
chr10:50881101
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-94+4480G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881101 | ||||||
chr10:50881102
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-94+4479C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881102 | ||||||
chr10:50881134
|
T | C | 1 | a0001c0001t0005g0240 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-94+4447A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881134 | ||||||
chr10:50881257
|
C | A | 5 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0010g0097others(2): Show | 7 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+4324G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881257 | ||||||
chr10:50881437
|
G | C | 2 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-94+4144C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881437 | ||||||
chr10:50881439
|
C | T | 26 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(23): Show | 33 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-94+4142G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881439 | ||||||
chr10:50881495
|
G | A | 1 | a0001c0001t0005g0243 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-94+4086C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881495 | ||||||
chr10:50881783
|
G | A | 5 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0010g0097others(2): Show | 7 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+3798C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881783 | ||||||
chr10:50881804
|
T | C | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.-94+3777A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881804 | ||||||
chr10:50881819
|
T | C | 2 | a0001c0001t0037g0050a0002c0004t0044g0049 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+3762A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881819 | ||||||
chr10:50881913
|
T | G | 1 | a0001c0002t0004g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-94+3668A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881913 | ||||||
chr10:50882028
|
T | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.-94+3553A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882028 | ||||||
chr10:50882282
|
A | G | 1 | a0001c0001t0005g0277 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-94+3299T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882282 | ||||||
chr10:50882624
|
A | G | 46 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(43): Show | 58 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-94+2957T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882624 | ||||||
chr10:50882740
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(60): Show | 73 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-94+2841G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882740 | ||||||
chr10:50882757
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-94+2824A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882757 | ||||||
chr10:50882847
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-94+2734A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882847 | ||||||
chr10:50882877
|
A | G | 3 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0010g0097 | 5 | HG01192.hp1 HG02258.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+2704T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882877 | ||||||
chr10:50883049
|
A | C | 1 | a0001c0001t0005g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-94+2532T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883049 | ||||||
chr10:50883139
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+2442C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883139 | ||||||
chr10:50883190
|
A | C | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+2391T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883190 | ||||||
chr10:50883278
|
T | C | 6 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0280others(3): Show | 6 | HG02280.hp1 HG03654.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94+2303A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883278 | ||||||
chr10:50883318
|
A | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(219): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-94+2263T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883318 | ||||||
chr10:50883419
|
C | T | 48 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(45): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-94+2162G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883419 | ||||||
chr10:50883461
|
T | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(219): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-94+2120A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883461 | ||||||
chr10:50883734
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-94+1847C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883734 | ||||||
chr10:50883803
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-94+1778G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883803 | ||||||
chr10:50884062
|
A | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-94+1519T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884062 | ||||||
chr10:50884065
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-94+1516G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884065 | ||||||
chr10:50884144
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-94+1437T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884144 | ||||||
chr10:50884203
|
A | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+1378T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884203 | ||||||
chr10:50884324
|
G | A | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-94+1257C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884324 | ||||||
chr10:50884559
|
A | T | 48 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(45): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-94+1022T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884559 | ||||||
chr10:50884611
|
C | T | 1 | a0001c0001t0028g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-94+970G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884611 | ||||||
chr10:50884712
|
A | T | 1 | a0001c0001t0002g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-94+869T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884712 | ||||||
chr10:50884716
|
T | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-94+865A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884716 | ||||||
chr10:50884750
|
C | T | 1 | a0001c0008t0001g0039 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-94+831G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884750 | ||||||
chr10:50884774
|
A | G | 3 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0261 | 3 | NA18994.hp1 NA19002.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-94+807T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884774 | ||||||
chr10:50884803
|
G | A | 5 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285others(2): Show | 5 | HG02602.hp2 NA18948.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+778C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884803 | ||||||
chr10:50884853
|
C | G | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+728G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884853 | ||||||
chr10:50884940
|
A | G | 1 | a0001c0001t0039g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-94+641T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884940 | ||||||
chr10:50885001
|
T | A | 12 | a0001c0001t0005g0251a0001c0001t0005g0253a0001c0001t0014g0252others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+580A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885001 | ||||||
chr10:50885072
|
G | A | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+509C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885072 | ||||||
chr10:50885137
|
A | T | 2 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+444T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885137 | ||||||
chr10:50885350
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-94+231G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885350 | ||||||
chr10:50885488
|
G | A | 34 | a0001c0001t0001g0276a0001c0001t0003g0033a0001c0001t0003g0259others(31): Show | 42 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-94+93C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885488 | ||||||
chr10:50885574
|
A | G | 1 | a0002c0004t0018g0034 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.-94+7T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885574 |