geneid | 1063 |
---|---|
ensemblid | ENSG00000117724.15 |
hgncid | 1857 |
symbol | CENPF |
name | centromere protein F |
refseq_nuc | NM_016343.4 |
refseq_prot | NP_057427.3 |
ensembl_nuc | ENST00000366955.8 |
ensembl_prot | ENSP00000355922.3 |
mane_status | MANE Select |
chr | chr1 |
start | 214603195 |
end | 214664571 |
strand | + |
ver | v1.2 |
region | chr1:214603195-214664571 |
region5000 | chr1:214598195-214669571 |
regionname0 | CENPF_chr1_214603195_214664571 |
regionname5000 | CENPF_chr1_214598195_214669571 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 3114 | 81 | 7 | 16 | 42 | 4 | 12 | 28 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002 | 0/1 | 3114 | 35 | 1 | 9 | 10 | 4 | 10 | 9 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0003 | 0/0 | 3114 | 27 | 0 | 5 | 17 | 0 | 5 | 13 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004 | 0/0 | 3114 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0005 | 0/0 | 3114 | 15 | 1 | 4 | 9 | 0 | 1 | 8 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0006 | 0/0 | 3114 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0007 | 1/0 | 3114 | 9 | 6 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0008 | 0/0 | 3114 | 8 | 2 | 1 | 4 | 1 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0009 | 0/0 | 3114 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0010 | 0/0 | 3114 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0011 | 0/0 | 3114 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0012 | 0/0 | 3114 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0013 | 0/0 | 3114 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0014 | 0/0 | 3114 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0015 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0016 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0017 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0018 | 0/0 | 3114 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0019 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0020 | 0/0 | 3114 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0021 | 0/0 | 3114 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0022 | 0/0 | 3114 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0023 | 0/0 | 3114 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0024 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0025 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0026 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0027 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0028 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0029 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0030 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0031 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0032 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0033 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0034 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0035 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0036 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0037 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0038 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0039 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0040 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0041 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0042 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0043 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0044 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0045 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0046 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0047 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0048 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0049 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0050 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 9345 | 73 | 7 | 16 | 39 | 4 | 7 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0002 | 0/1 | 9345 | 34 | 1 | 8 | 10 | 4 | 10 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0003 | 0/0 | 9345 | 26 | 0 | 5 | 17 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0004 | 0/0 | 9345 | 16 | 15 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0005 | 0/0 | 9345 | 15 | 1 | 4 | 9 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0006 | 0/0 | 9345 | 8 | 2 | 1 | 4 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0007 | 0/0 | 9345 | 8 | 8 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0008 | 0/0 | 9345 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0009 | 1/0 | 9345 | 5 | 2 | 0 | 1 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0010 | 0/0 | 9345 | 5 | 5 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0011 | 0/0 | 9345 | 4 | 0 | 0 | 0 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0012 | 0/0 | 9345 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0013 | 0/0 | 9345 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0014 | 0/0 | 9345 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0015 | 0/0 | 9345 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0016 | 0/0 | 9345 | 3 | 0 | 3 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0017 | 0/0 | 9345 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0018 | 0/0 | 9345 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0019 | 0/0 | 9345 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0020 | 0/0 | 9345 | 3 | 1 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0021 | 0/0 | 9345 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0022 | 0/0 | 9345 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0023 | 0/0 | 9345 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0024 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0025 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0026 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0027 | 0/0 | 9345 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0028 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0029 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0030 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0031 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0032 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0033 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0034 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0035 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0036 | 0/0 | 9345 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0037 | 0/0 | 9345 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0038 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0039 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0040 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0041 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0042 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0043 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0044 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0045 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0046 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0047 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0048 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0049 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0050 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0051 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0052 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0053 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0054 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0055 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0056 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0057 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0058 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0059 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0060 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0061 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
c0062 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 946 | 154 | 28 | 30 | 60 | 11 | 23 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0002 | 0/0 | 946 | 83 | 50 | 9 | 20 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0003 | 0/0 | 946 | 17 | 1 | 6 | 9 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0004 | 0/0 | 946 | 11 | 10 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0005 | 0/0 | 946 | 4 | 0 | 1 | 0 | 0 | 3 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0006 | 0/0 | 946 | 4 | 1 | 0 | 0 | 0 | 3 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0007 | 0/0 | 946 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0008 | 0/0 | 946 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0009 | 0/0 | 946 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0010 | 0/0 | 946 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0011 | 0/0 | 946 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0012 | 0/0 | 946 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0013 | 0/0 | 946 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
t0014 | 0/0 | 946 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 9345 | 73 | 7 | 16 | 39 | 4 | 7 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0011 | 0/0 | 9345 | 4 | 0 | 0 | 0 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0017 | 0/0 | 9345 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0042 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0002 | 0/1 | 9345 | 34 | 1 | 8 | 10 | 4 | 10 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0032 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0003c0003 | 0/0 | 9345 | 26 | 0 | 5 | 17 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0003c0059 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004c0004 | 0/0 | 9345 | 16 | 15 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004c0013 | 0/0 | 9345 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004c0033 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0005c0005 | 0/0 | 9345 | 15 | 1 | 4 | 9 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0006c0007 | 0/0 | 9345 | 8 | 8 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0006c0030 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0007c0009 | 1/0 | 9345 | 5 | 2 | 0 | 1 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0007c0012 | 0/0 | 9345 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0008c0006 | 0/0 | 9345 | 8 | 2 | 1 | 4 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0009c0010 | 0/0 | 9345 | 5 | 5 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0010c0008 | 0/0 | 9345 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0011c0018 | 0/0 | 9345 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0011c0034 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0012c0014 | 0/0 | 9345 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0013c0015 | 0/0 | 9345 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0014c0016 | 0/0 | 9345 | 3 | 0 | 3 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0015c0019 | 0/0 | 9345 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0016c0029 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0016c0052 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0017c0024 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0017c0055 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0018c0020 | 0/0 | 9345 | 3 | 1 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0019c0025 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0020c0021 | 0/0 | 9345 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0021c0022 | 0/0 | 9345 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0022c0027 | 0/0 | 9345 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0023c0023 | 0/0 | 9345 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0024c0028 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0025c0026 | 0/0 | 9345 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0026c0062 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0027c0038 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0028c0040 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0029c0039 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0030c0031 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0031c0037 | 0/0 | 9345 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0032c0041 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0033c0036 | 0/0 | 9345 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0034c0054 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0035c0035 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0036c0049 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0037c0050 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0038c0051 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0039c0053 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0040c0047 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0041c0048 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0042c0046 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0043c0043 | 0/0 | 9345 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0044c0045 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0045c0044 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0046c0058 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0047c0056 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0048c0057 | 0/0 | 9345 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0049c0060 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0050c0061 | 0/0 | 9345 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10290 | 70 | 7 | 16 | 36 | 4 | 7 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0001t0008 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0001t0009 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0001t0011 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0011t0001 | 0/0 | 10290 | 4 | 0 | 0 | 0 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0017t0001 | 0/0 | 10290 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0001c0042t0001 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0002t0001 | 0/1 | 10290 | 25 | 1 | 6 | 7 | 4 | 6 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0002t0002 | 0/0 | 10290 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0002t0005 | 0/0 | 10290 | 4 | 0 | 1 | 0 | 0 | 3 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0002t0007 | 0/0 | 10290 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0002c0032t0001 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0003c0003t0002 | 0/0 | 10290 | 25 | 0 | 5 | 17 | 0 | 3 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0003c0003t0013 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0003c0059t0002 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004c0004t0002 | 0/0 | 10290 | 16 | 15 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004c0013t0002 | 0/0 | 10290 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0004c0033t0002 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0005c0005t0003 | 0/0 | 10290 | 15 | 1 | 4 | 9 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0006c0007t0002 | 0/0 | 10290 | 8 | 8 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0006c0030t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0007c0009t0001 | 1/0 | 10290 | 5 | 2 | 0 | 1 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0007c0012t0001 | 0/0 | 10290 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0008c0006t0001 | 0/0 | 10290 | 8 | 2 | 1 | 4 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0009c0010t0001 | 0/0 | 10290 | 5 | 5 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0010c0008t0001 | 0/0 | 10290 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0011c0018t0002 | 0/0 | 10290 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0011c0034t0014 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0012c0014t0002 | 0/0 | 10290 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0013c0015t0004 | 0/0 | 10290 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0014c0016t0001 | 0/0 | 10290 | 3 | 0 | 3 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0015c0019t0001 | 0/0 | 10290 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0016c0029t0004 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0016c0052t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0017c0024t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0017c0055t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0018c0020t0006 | 0/0 | 10290 | 3 | 1 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0019c0025t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0019c0025t0012 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0020c0021t0001 | 0/0 | 10290 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0021c0022t0001 | 0/0 | 10290 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0022c0027t0001 | 0/0 | 10290 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0023c0023t0001 | 0/0 | 10290 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0024c0028t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0025c0026t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0026c0062t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0027c0038t0001 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0028c0040t0010 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0029c0039t0001 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0030c0031t0001 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0031c0037t0001 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0032c0041t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0033c0036t0001 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0034c0054t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0035c0035t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0036c0049t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0037c0050t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0038c0051t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0039c0053t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0040c0047t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0041c0048t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0042c0046t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0043c0043t0006 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0044c0045t0003 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0045c0044t0003 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0046c0058t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0047c0056t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0048c0057t0002 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0049c0060t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
a0050c0061t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | copy fasta | chr1 | 214598195 | 214669571 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0017t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0017t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0017t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0042t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0032t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0013g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0059t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0033t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0030t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0030t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0012t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0012t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0012t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0018t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0018t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0018t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0034t0014g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0014t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0014t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0014t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0014t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0015t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0015t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0015t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0015t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0014c0016t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0014c0016t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0014c0016t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0015c0019t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0015c0019t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0015c0019t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0016c0029t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0016c0029t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0016c0052t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0017c0024t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0017c0024t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0017c0055t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0018c0020t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0018c0020t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0018c0020t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0019c0025t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0019c0025t0012g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0020c0021t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0020c0021t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0021c0022t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0021c0022t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0022c0027t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0022c0027t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0023c0023t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0023c0023t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0024c0028t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0024c0028t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0025c0026t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0025c0026t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0026c0062t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0027c0038t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0028c0040t0010g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0029c0039t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0030c0031t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0031c0037t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0032c0041t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0033c0036t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0034c0054t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0035c0035t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0036c0049t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0037c0050t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0038c0051t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0039c0053t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0040c0047t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0041c0048t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0042c0046t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0043c0043t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0044c0045t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0045c0044t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0046c0058t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0047c0056t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0048c0057t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0049c0060t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0050c0061t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0091 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0190 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00323 | hp2 | a0021 | c0022 | t0001 | g0108 | EUR | FIN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0194 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00408 | hp2 | a0003 | c0003 | t0002 | g0062 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00639 | hp2 | a0002 | c0002 | t0005 | g0095 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00642 | hp1 | a0002 | c0032 | t0001 | g0119 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00642 | hp2 | a0004 | c0033 | t0002 | g0028 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00673 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01074 | hp1 | a0003 | c0003 | t0002 | g0066 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01081 | hp2 | a0022 | c0027 | t0001 | g0131 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01106 | hp1 | a0012 | c0014 | t0002 | g0022 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01109 | hp1 | a0004 | c0004 | t0002 | g0216 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01109 | hp2 | a0013 | c0015 | t0004 | g0051 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01192 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01192 | hp2 | a0014 | c0016 | t0001 | g0167 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01257 | hp2 | a0003 | c0003 | t0002 | g0072 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01258 | hp2 | a0003 | c0003 | t0002 | g0008 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01346 | hp2 | a0005 | c0005 | t0003 | g0252 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01358 | hp1 | a0045 | c0044 | t0003 | g0239 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01433 | hp1 | a0029 | c0039 | t0001 | g0181 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01433 | hp2 | a0002 | c0002 | t0007 | g0125 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01496 | hp1 | a0005 | c0005 | t0003 | g0016 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0113 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01515 | hp2 | a0030 | c0031 | t0001 | g0202 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0189 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01891 | hp1 | a0006 | c0007 | t0002 | g0045 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01891 | hp2 | a0011 | c0034 | t0014 | g0029 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01928 | hp2 | a0005 | c0005 | t0003 | g0016 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01978 | hp2 | a0014 | c0016 | t0001 | g0175 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01981 | hp1 | a0021 | c0022 | t0001 | g0115 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01981 | hp2 | a0014 | c0016 | t0001 | g0183 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01993 | hp1 | a0005 | c0005 | t0003 | g0250 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01993 | hp2 | a0044 | c0045 | t0003 | g0240 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02004 | hp2 | a0048 | c0057 | t0002 | g0007 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02055 | hp1 | a0009 | c0010 | t0001 | g0171 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02055 | hp2 | a0047 | c0056 | t0002 | g0026 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02080 | hp1 | a0003 | c0003 | t0002 | g0070 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02135 | hp1 | a0001 | c0017 | t0001 | g0182 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02135 | hp2 | a0003 | c0003 | t0002 | g0060 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02145 | hp1 | a0035 | c0035 | t0002 | g0030 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02145 | hp2 | a0004 | c0004 | t0002 | g0228 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02257 | hp1 | a0013 | c0015 | t0004 | g0052 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02257 | hp2 | a0024 | c0028 | t0002 | g0233 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02273 | hp1 | a0008 | c0006 | t0001 | g0124 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02273 | hp2 | a0003 | c0003 | t0002 | g0063 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02280 | hp1 | a0006 | c0007 | t0002 | g0036 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02280 | hp2 | a0036 | c0049 | t0004 | g0049 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02451 | hp1 | a0016 | c0029 | t0004 | g0017 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02451 | hp2 | a0019 | c0025 | t0002 | g0236 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02523 | hp1 | a0005 | c0005 | t0003 | g0251 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02523 | hp2 | a0033 | c0036 | t0001 | g0094 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02572 | hp1 | a0004 | c0004 | t0002 | g0230 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02615 | hp1 | a0012 | c0014 | t0002 | g0023 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02615 | hp2 | a0015 | c0019 | t0001 | g0079 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02622 | hp1 | a0008 | c0006 | t0001 | g0096 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02622 | hp2 | a0007 | c0012 | t0001 | g0010 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02630 | hp1 | a0019 | c0025 | t0012 | g0237 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02630 | hp2 | a0011 | c0018 | t0002 | g0238 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02647 | hp2 | a0004 | c0004 | t0002 | g0231 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02698 | hp2 | a0002 | c0002 | t0005 | g0106 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02717 | hp1 | a0004 | c0013 | t0002 | g0033 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02717 | hp2 | a0009 | c0010 | t0001 | g0159 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02723 | hp1 | a0009 | c0010 | t0001 | g0144 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02809 | hp1 | a0007 | c0012 | t0001 | g0010 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02809 | hp2 | a0050 | c0061 | t0004 | g0057 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02886 | hp1 | a0012 | c0014 | t0002 | g0020 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02886 | hp2 | a0015 | c0019 | t0001 | g0081 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02895 | hp1 | a0007 | c0009 | t0001 | g0158 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02895 | hp2 | a0004 | c0004 | t0002 | g0218 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02896 | hp1 | a0004 | c0004 | t0002 | g0220 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02896 | hp2 | a0006 | c0030 | t0002 | g0037 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02897 | hp1 | a0006 | c0030 | t0002 | g0039 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02897 | hp2 | a0004 | c0004 | t0002 | g0217 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02922 | hp1 | a0011 | c0018 | t0002 | g0232 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02922 | hp2 | a0013 | c0015 | t0004 | g0050 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02965 | hp1 | a0004 | c0013 | t0002 | g0031 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02965 | hp2 | a0011 | c0018 | t0002 | g0225 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02970 | hp1 | a0015 | c0019 | t0001 | g0080 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02970 | hp2 | a0004 | c0004 | t0002 | g0227 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02976 | hp1 | a0024 | c0028 | t0002 | g0234 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02976 | hp2 | a0006 | c0007 | t0002 | g0040 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03017 | hp1 | a0023 | c0023 | t0001 | g0084 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03041 | hp2 | a0038 | c0051 | t0001 | g0205 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03098 | hp1 | a0004 | c0013 | t0002 | g0035 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03098 | hp2 | a0007 | c0012 | t0001 | g0085 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03130 | hp1 | a0007 | c0012 | t0001 | g0128 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03130 | hp2 | a0008 | c0006 | t0001 | g0104 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03139 | hp1 | a0039 | c0053 | t0004 | g0056 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03139 | hp2 | a0025 | c0026 | t0002 | g0048 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03195 | hp1 | a0046 | c0058 | t0002 | g0025 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03195 | hp2 | a0017 | c0024 | t0002 | g0047 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03209 | hp1 | a0040 | c0047 | t0002 | g0034 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03209 | hp2 | a0006 | c0007 | t0002 | g0043 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03225 | hp1 | a0004 | c0004 | t0002 | g0235 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03225 | hp2 | a0006 | c0007 | t0002 | g0042 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03239 | hp1 | a0001 | c0042 | t0001 | g0001 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03239 | hp2 | a0018 | c0020 | t0006 | g0215 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03453 | hp1 | a0042 | c0046 | t0002 | g0027 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03453 | hp2 | a0013 | c0015 | t0004 | g0053 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03491 | hp1 | a0003 | c0059 | t0002 | g0069 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03491 | hp2 | a0001 | c0011 | t0001 | g0126 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03492 | hp2 | a0001 | c0011 | t0001 | g0160 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03516 | hp1 | a0032 | c0041 | t0001 | g0204 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03516 | hp2 | a0004 | c0004 | t0002 | g0226 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03540 | hp1 | a0026 | c0062 | t0001 | g0145 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03540 | hp2 | a0025 | c0026 | t0002 | g0024 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03579 | hp1 | a0009 | c0010 | t0001 | g0143 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03579 | hp2 | a0006 | c0007 | t0002 | g0041 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03654 | hp1 | a0001 | c0011 | t0001 | g0012 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03688 | hp1 | a0003 | c0003 | t0013 | g0068 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03704 | hp1 | a0002 | c0002 | t0005 | g0009 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03704 | hp2 | a0043 | c0043 | t0006 | g0246 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03710 | hp2 | a0027 | c0038 | t0001 | g0138 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03831 | hp1 | a0005 | c0005 | t0003 | g0249 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03831 | hp2 | a0003 | c0003 | t0002 | g0058 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03834 | hp1 | a0018 | c0020 | t0006 | g0214 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03834 | hp2 | a0002 | c0002 | t0005 | g0118 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03927 | hp1 | a0023 | c0023 | t0001 | g0191 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03927 | hp2 | a0007 | c0009 | t0001 | g0180 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04115 | hp2 | a0001 | c0011 | t0001 | g0136 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04199 | hp2 | a0022 | c0027 | t0001 | g0132 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0067 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18522 | hp1 | a0017 | c0024 | t0002 | g0046 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18612 | hp1 | a0007 | c0009 | t0001 | g0186 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18906 | hp1 | a0041 | c0048 | t0002 | g0223 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18906 | hp2 | a0034 | c0054 | t0002 | g0211 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18941 | hp1 | a0020 | c0021 | t0001 | g0116 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18941 | hp2 | a0003 | c0003 | t0002 | g0059 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0073 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18943 | hp1 | a0005 | c0005 | t0003 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18943 | hp2 | a0010 | c0008 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18950 | hp1 | a0010 | c0008 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18952 | hp1 | a0005 | c0005 | t0003 | g0244 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18952 | hp2 | a0001 | c0001 | t0011 | g0200 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18962 | hp2 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18964 | hp1 | a0008 | c0006 | t0001 | g0123 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18965 | hp1 | a0008 | c0006 | t0001 | g0083 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18965 | hp2 | a0008 | c0006 | t0001 | g0121 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18969 | hp1 | a0001 | c0017 | t0001 | g0155 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18973 | hp2 | a0005 | c0005 | t0003 | g0247 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18979 | hp1 | a0003 | c0003 | t0002 | g0061 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18982 | hp1 | a0005 | c0005 | t0003 | g0245 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18988 | hp2 | a0020 | c0021 | t0001 | g0192 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18989 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18990 | hp1 | a0010 | c0008 | t0001 | g0077 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18994 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18998 | hp1 | a0005 | c0005 | t0003 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18998 | hp2 | a0010 | c0008 | t0001 | g0099 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19010 | hp2 | a0003 | c0003 | t0002 | g0065 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19011 | hp1 | a0031 | c0037 | t0001 | g0164 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19011 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19012 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19030 | hp2 | a0016 | c0052 | t0001 | g0169 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19043 | hp1 | a0004 | c0004 | t0002 | g0222 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19043 | hp2 | a0004 | c0013 | t0002 | g0032 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19054 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19074 | hp1 | a0005 | c0005 | t0003 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19074 | hp2 | a0001 | c0017 | t0001 | g0174 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19082 | hp2 | a0005 | c0005 | t0003 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19091 | hp1 | a0010 | c0008 | t0001 | g0100 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19091 | hp2 | a0005 | c0005 | t0003 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19240 | hp1 | a0049 | c0060 | t0004 | g0054 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19240 | hp2 | a0009 | c0010 | t0001 | g0139 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0229 | AFR | ASW | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20752 | hp1 | a0028 | c0040 | t0010 | g0146 | EUR | TSI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20752 | hp2 | a0008 | c0006 | t0001 | g0107 | EUR | TSI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20905 | hp1 | a0002 | c0002 | t0007 | g0114 | SAS | GIH | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20905 | hp2 | a0003 | c0003 | t0002 | g0008 | SAS | GIH | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02109 | hp1 | a0017 | c0055 | t0002 | g0019 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02109 | hp2 | a0006 | c0007 | t0002 | g0038 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02486 | hp1 | a0018 | c0020 | t0006 | g0213 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02486 | hp2 | a0004 | c0004 | t0002 | g0219 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02559 | hp1 | a0012 | c0014 | t0002 | g0021 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02559 | hp2 | a0004 | c0004 | t0002 | g0212 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03471 | hp1 | a0006 | c0007 | t0002 | g0044 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03471 | hp2 | a0016 | c0029 | t0004 | g0018 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG06807 | hp1 | a0037 | c0050 | t0004 | g0055 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG06807 | hp2 | a0004 | c0004 | t0002 | g0221 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18955 | hp1 | a0008 | c0006 | t0001 | g0120 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18955 | hp2 | a0003 | c0003 | t0002 | g0074 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20300 | hp1 | a0005 | c0005 | t0003 | g0248 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20300 | hp2 | a0007 | c0009 | t0001 | g0133 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA21309 | hp1 | a0004 | c0004 | t0002 | g0224 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0105 | REF | REF | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
homoSapiens_grch38 | hp1 | a0007 | c0009 | t0001 | g0178 | REF | REF | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214622111
|
C | T | 2 | a0009a0026 | 6 | HG02055.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.898C>T | p.Arg300Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/20 | 1066/10290 | 898/9345 | 300/3114 | chr1 | 214622111 | ||
chr1:214622268
|
A | G | 1 | a0050 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1055A>G | p.Gln352Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/20 | 1223/10290 | 1055/9345 | 352/3114 | chr1 | 214622268 | ||
chr1:214629122
|
G | A | 1 | a0019 | 2 | HG02451.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.1145G>A | p.Arg382Lys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/20 | 1313/10290 | 1145/9345 | 382/3114 | chr1 | 214629122 | ||
chr1:214630582
|
A | C | 2 | a0013a0049 | 5 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.1243A>C | p.Ile415Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/20 | 1411/10290 | 1243/9345 | 415/3114 | chr1 | 214630582 | ||
chr1:214637901
|
C | G | 31 | a0003a0004a0005others(28): Show | 120 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(117): Show |
missense_variant | MODERATE | c.1482C>G | p.His494Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/20 | 1650/10290 | 1482/9345 | 494/3114 | chr1 | 214637901 | ||
chr1:214640043
|
T | C | 1 | a0033 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1705T>C | p.Cys569Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 1873/10290 | 1705/9345 | 569/3114 | chr1 | 214640043 | ||
chr1:214640439
|
A | C | 2 | a0015a0034 | 4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.2101A>C | p.Met701Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2269/10290 | 2101/9345 | 701/3114 | chr1 | 214640439 | ||
chr1:214640439
|
A | G | 7 | a0003a0017a0018others(4): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.2101A>G | p.Met701Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2269/10290 | 2101/9345 | 701/3114 | chr1 | 214640439 | ||
chr1:214640598
|
C | G | 7 | a0003a0017a0018others(4): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.2260C>G | p.Gln754Glu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2428/10290 | 2260/9345 | 754/3114 | chr1 | 214640598 | ||
chr1:214640716
|
T | G | 4 | a0005a0043a0044others(1): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
missense_variant | MODERATE | c.2378T>G | p.Met793Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2546/10290 | 2378/9345 | 793/3114 | chr1 | 214640716 | ||
chr1:214640782
|
G | A | 7 | a0003a0017a0018others(4): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.2444G>A | p.Arg815His | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2612/10290 | 2444/9345 | 815/3114 | chr1 | 214640782 | ||
chr1:214641390
|
T | G | 7 | a0003a0017a0018others(4): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.3052T>G | p.Tyr1018Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3220/10290 | 3052/9345 | 1018/3114 | chr1 | 214641390 | ||
chr1:214641435
|
G | A | 11 | a0003a0006a0012others(8): Show | 56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
missense_variant | MODERATE | c.3097G>A | p.Gly1033Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3265/10290 | 3097/9345 | 1033/3114 | chr1 | 214641435 | ||
chr1:214641451
|
A | G | 1 | a0042 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3113A>G | p.Asp1038Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3281/10290 | 3113/9345 | 1038/3114 | chr1 | 214641451 | ||
chr1:214641582
|
C | T | 1 | a0018 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.3244C>T | p.His1082Tyr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3412/10290 | 3244/9345 | 1082/3114 | chr1 | 214641582 | ||
chr1:214641652
|
C | T | 7 | a0003a0017a0018others(4): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.3314C>T | p.Thr1105Ile | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3482/10290 | 3314/9345 | 1105/3114 | chr1 | 214641652 | ||
chr1:214641773
|
A | T | 4 | a0006a0012a0015others(1): Show | 18 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
missense_variant | MODERATE | c.3435A>T | p.Glu1145Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3603/10290 | 3435/9345 | 1145/3114 | chr1 | 214641773 | ||
chr1:214641961
|
C | T | 2 | a0044a0045 | 2 | HG01358.hp1 HG01993.hp2 |
missense_variant | MODERATE | c.3623C>T | p.Ala1208Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3791/10290 | 3623/9345 | 1208/3114 | chr1 | 214641961 | ||
chr1:214642266
|
C | G | 1 | a0025 | 2 | HG03139.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.3928C>G | p.Leu1310Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4096/10290 | 3928/9345 | 1310/3114 | chr1 | 214642266 | ||
chr1:214642573
|
T | C | 7 | a0003a0017a0018others(4): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.4235T>C | p.Leu1412Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4403/10290 | 4235/9345 | 1412/3114 | chr1 | 214642573 | ||
chr1:214642627
|
C | G | 1 | a0046 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.4289C>G | p.Ser1430Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4457/10290 | 4289/9345 | 1430/3114 | chr1 | 214642627 | ||
chr1:214642881
|
G | A | 30 | a0003a0004a0005others(27): Show | 119 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(116): Show |
missense_variant | MODERATE | c.4543G>A | p.Ala1515Thr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4711/10290 | 4543/9345 | 1515/3114 | chr1 | 214642881 | ||
chr1:214642954
|
A | G | 2 | a0003a0048 | 28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
missense_variant | MODERATE | c.4616A>G | p.Lys1539Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4784/10290 | 4616/9345 | 1539/3114 | chr1 | 214642954 | ||
chr1:214643295
|
C | T | 1 | a0048 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.4957C>T | p.Arg1653Trp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 5125/10290 | 4957/9345 | 1653/3114 | chr1 | 214643295 | ||
chr1:214644678
|
A | G | 4 | a0006a0012a0015others(1): Show | 18 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
missense_variant | MODERATE | c.5108A>G | p.Asn1703Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5276/10290 | 5108/9345 | 1703/3114 | chr1 | 214644678 | ||
chr1:214644872
|
G | A | 8 | a0003a0017a0018others(5): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.5302G>A | p.Asp1768Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5470/10290 | 5302/9345 | 1768/3114 | chr1 | 214644872 | ||
chr1:214644880
|
T | A | 20 | a0003a0004a0005others(17): Show | 101 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(98): Show |
missense_variant | MODERATE | c.5310T>A | p.His1770Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5478/10290 | 5310/9345 | 1770/3114 | chr1 | 214644880 | ||
chr1:214644903
|
A | G | 1 | a0041 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.5333A>G | p.Glu1778Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5501/10290 | 5333/9345 | 1778/3114 | chr1 | 214644903 | ||
chr1:214644963
|
A | G | 1 | a0032 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.5393A>G | p.Glu1798Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5561/10290 | 5393/9345 | 1798/3114 | chr1 | 214644963 | ||
chr1:214645205
|
C | T | 1 | a0018 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.5635C>T | p.Arg1879Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5803/10290 | 5635/9345 | 1879/3114 | chr1 | 214645205 | ||
chr1:214645284
|
G | A | 1 | a0036 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.5714G>A | p.Ser1905Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5882/10290 | 5714/9345 | 1905/3114 | chr1 | 214645284 | ||
chr1:214645461
|
G | A | 1 | a0037 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.5891G>A | p.Arg1964His | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6059/10290 | 5891/9345 | 1964/3114 | chr1 | 214645461 | ||
chr1:214645494
|
C | T | 2 | a0015a0034 | 4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.5924C>T | p.Thr1975Met | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6092/10290 | 5924/9345 | 1975/3114 | chr1 | 214645494 | ||
chr1:214645503
|
A | G | 8 | a0003a0017a0018others(5): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.5933A>G | p.Asp1978Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6101/10290 | 5933/9345 | 1978/3114 | chr1 | 214645503 | ||
chr1:214645569
|
A | G | 1 | a0039 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.5999A>G | p.His2000Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6167/10290 | 5999/9345 | 2000/3114 | chr1 | 214645569 | ||
chr1:214645602
|
A | C | 9 | a0003a0017a0018others(6): Show | 42 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(39): Show |
missense_variant | MODERATE | c.6032A>C | p.Glu2011Ala | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6200/10290 | 6032/9345 | 2011/3114 | chr1 | 214645602 | ||
chr1:214645701
|
C | T | 6 | a0017a0018a0019others(3): Show | 12 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
missense_variant | MODERATE | c.6131C>T | p.Ser2044Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6299/10290 | 6131/9345 | 2044/3114 | chr1 | 214645701 | ||
chr1:214645785
|
C | A | 1 | a0049 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6215C>A | p.Ser2072Tyr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6383/10290 | 6215/9345 | 2072/3114 | chr1 | 214645785 | ||
chr1:214645985
|
G | A | 8 | a0003a0017a0018others(5): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.6415G>A | p.Ala2139Thr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6583/10290 | 6415/9345 | 2139/3114 | chr1 | 214645985 | ||
chr1:214646003
|
C | T | 1 | a0015 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.6433C>T | p.Arg2145Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6601/10290 | 6433/9345 | 2145/3114 | chr1 | 214646003 | ||
chr1:214646043
|
A | G | 1 | a0023 | 2 | HG03017.hp1 HG03927.hp1 |
missense_variant | MODERATE | c.6473A>G | p.Asn2158Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6641/10290 | 6473/9345 | 2158/3114 | chr1 | 214646043 | ||
chr1:214646173
|
T | G | 1 | a0031 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.6603T>G | p.Phe2201Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6771/10290 | 6603/9345 | 2201/3114 | chr1 | 214646173 | ||
chr1:214646244
|
A | G | 8 | a0003a0017a0018others(5): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.6674A>G | p.Gln2225Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6842/10290 | 6674/9345 | 2225/3114 | chr1 | 214646244 | ||
chr1:214646438
|
G | A | 1 | a0040 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.6868G>A | p.Asp2290Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7036/10290 | 6868/9345 | 2290/3114 | chr1 | 214646438 | ||
chr1:214646439
|
A | T | 1 | a0040 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.6869A>T | p.Asp2290Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7037/10290 | 6869/9345 | 2290/3114 | chr1 | 214646439 | ||
chr1:214646475
|
G | A | 1 | a0020 | 2 | NA18941.hp1 NA18988.hp2 |
missense_variant | MODERATE | c.6905G>A | p.Ser2302Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7073/10290 | 6905/9345 | 2302/3114 | chr1 | 214646475 | ||
chr1:214646507
|
G | A | 1 | a0030 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.6937G>A | p.Asp2313Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7105/10290 | 6937/9345 | 2313/3114 | chr1 | 214646507 | ||
chr1:214646637
|
C | T | 8 | a0003a0017a0018others(5): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.7067C>T | p.Ala2356Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7235/10290 | 7067/9345 | 2356/3114 | chr1 | 214646637 | ||
chr1:214646736
|
C | G | 1 | a0047 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.7166C>G | p.Thr2389Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7334/10290 | 7166/9345 | 2389/3114 | chr1 | 214646736 | ||
chr1:214646756
|
A | G | 7 | a0002a0008a0010others(4): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
missense_variant | MODERATE | c.7186A>G | p.Asn2396Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7354/10290 | 7186/9345 | 2396/3114 | chr1 | 214646756 | ||
chr1:214646896
|
G | A | 1 | a0025 | 2 | HG03139.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.7326G>A | p.Met2442Ile | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7494/10290 | 7326/9345 | 2442/3114 | chr1 | 214646896 | ||
chr1:214647125
|
A | G | 1 | a0015 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.7555A>G | p.Lys2519Glu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7723/10290 | 7555/9345 | 2519/3114 | chr1 | 214647125 | ||
chr1:214647227
|
G | A | 1 | a0010 | 5 | NA18943.hp2 NA18950.hp1 NA18990.hp1 others(2): Show |
missense_variant | MODERATE | c.7657G>A | p.Glu2553Lys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7825/10290 | 7657/9345 | 2553/3114 | chr1 | 214647227 | ||
chr1:214647339
|
A | T | 1 | a0044 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.7769A>T | p.Tyr2590Phe | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7937/10290 | 7769/9345 | 2590/3114 | chr1 | 214647339 | ||
chr1:214652853
|
G | A | 20 | a0001a0003a0005others(17): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
missense_variant | MODERATE | c.8186G>A | p.Arg2729Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/20 | 8354/10290 | 8186/9345 | 2729/3114 | chr1 | 214652853 | ||
chr1:214657274
|
A | G | 26 | a0001a0003a0005others(23): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
missense_variant | MODERATE | c.8827A>G | p.Arg2943Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/20 | 8995/10290 | 8827/9345 | 2943/3114 | chr1 | 214657274 | ||
chr1:214663730
|
G | A | 1 | a0029 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.9281G>A | p.Arg3094Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 9449/10290 | 9281/9345 | 3094/3114 | chr1 | 214663730 | ||
chr1:214663767
|
C | G | 29 | a0001a0003a0005others(26): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
missense_variant | MODERATE | c.9318C>G | p.Asn3106Lys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 9486/10290 | 9318/9345 | 3106/3114 | chr1 | 214663767 | ||
chr1:214663768
|
G | A | 1 | a0038 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.9319G>A | p.Gly3107Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 9487/10290 | 9319/9345 | 3107/3114 | chr1 | 214663768 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214613787
|
G | A | 8 | a0002c0002a0002c0032a0008c0006others(5): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
synonymous_variant | LOW | c.33G>A | p.Gly11Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/20 | 201/10290 | 33/9345 | 11/3114 | chr1 | 214613787 | ||
chr1:214619209
|
T | C | 1 | a0017c0024 | 2 | HG03195.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.562T>C | p.Leu188Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/20 | 730/10290 | 562/9345 | 188/3114 | chr1 | 214619209 | ||
chr1:214620936
|
G | A | 3 | a0004c0033a0011c0034a0035c0035 | 3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
synonymous_variant | LOW | c.855G>A | p.Ala285Ala | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/20 | 1023/10290 | 855/9345 | 285/3114 | chr1 | 214620936 | ||
chr1:214630557
|
T | G | 1 | a0025c0026 | 2 | HG03139.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.1218T>G | p.Ser406Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/20 | 1386/10290 | 1218/9345 | 406/3114 | chr1 | 214630557 | ||
chr1:214630596
|
C | G | 1 | a0025c0026 | 2 | HG03139.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.1257C>G | p.Ala419Ala | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/20 | 1425/10290 | 1257/9345 | 419/3114 | chr1 | 214630596 | ||
chr1:214640144
|
A | G | 14 | a0003c0003a0003c0059a0006c0007others(11): Show | 56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
synonymous_variant | LOW | c.1806A>G | p.Leu602Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 1974/10290 | 1806/9345 | 602/3114 | chr1 | 214640144 | ||
chr1:214640352
|
A | C | 1 | a0001c0042 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2014A>C | p.Arg672Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2182/10290 | 2014/9345 | 672/3114 | chr1 | 214640352 | ||
chr1:214641228
|
C | T | 8 | a0002c0002a0002c0032a0008c0006others(5): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
synonymous_variant | LOW | c.2890C>T | p.Leu964Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3058/10290 | 2890/9345 | 964/3114 | chr1 | 214641228 | ||
chr1:214641239
|
G | A | 9 | a0003c0003a0003c0059a0017c0024others(6): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
synonymous_variant | LOW | c.2901G>A | p.Arg967Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3069/10290 | 2901/9345 | 967/3114 | chr1 | 214641239 | ||
chr1:214641414
|
C | T | 1 | a0002c0032 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.3076C>T | p.Leu1026Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3244/10290 | 3076/9345 | 1026/3114 | chr1 | 214641414 | ||
chr1:214641440
|
T | C | 1 | a0042c0046 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.3102T>C | p.Asn1034Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3270/10290 | 3102/9345 | 1034/3114 | chr1 | 214641440 | ||
chr1:214641461
|
A | G | 1 | a0012c0014 | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.3123A>G | p.Gln1041Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3291/10290 | 3123/9345 | 1041/3114 | chr1 | 214641461 | ||
chr1:214641645
|
T | C | 1 | a0001c0011 | 4 | HG03491.hp2 HG03492.hp2 HG03654.hp1 others(1): Show |
synonymous_variant | LOW | c.3307T>C | p.Leu1103Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3475/10290 | 3307/9345 | 1103/3114 | chr1 | 214641645 | ||
chr1:214641707
|
C | T | 1 | a0003c0059 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.3369C>T | p.Ser1123Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3537/10290 | 3369/9345 | 1123/3114 | chr1 | 214641707 | ||
chr1:214642289
|
C | T | 1 | a0001c0017 | 3 | HG02135.hp1 NA18969.hp1 NA19074.hp2 |
synonymous_variant | LOW | c.3951C>T | p.Leu1317Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4119/10290 | 3951/9345 | 1317/3114 | chr1 | 214642289 | ||
chr1:214642799
|
T | G | 9 | a0003c0003a0003c0059a0017c0024others(6): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
synonymous_variant | LOW | c.4461T>G | p.Leu1487Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4629/10290 | 4461/9345 | 1487/3114 | chr1 | 214642799 | ||
chr1:214646539
|
A | G | 2 | a0004c0013a0040c0047 | 5 | HG02717.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.6969A>G | p.Gln2323Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7137/10290 | 6969/9345 | 2323/3114 | chr1 | 214646539 | ||
chr1:214646956
|
A | G | 10 | a0003c0003a0003c0059a0017c0024others(7): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
synonymous_variant | LOW | c.7386A>G | p.Glu2462Glu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7554/10290 | 7386/9345 | 2462/3114 | chr1 | 214646956 | ||
chr1:214647076
|
A | G | 2 | a0004c0013a0040c0047 | 5 | HG02717.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.7506A>G | p.Ser2502Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7674/10290 | 7506/9345 | 2502/3114 | chr1 | 214647076 | ||
chr1:214647151
|
G | A | 10 | a0003c0003a0003c0059a0017c0024others(7): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
synonymous_variant | LOW | c.7581G>A | p.Leu2527Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7749/10290 | 7581/9345 | 2527/3114 | chr1 | 214647151 | ||
chr1:214647181
|
T | C | 10 | a0003c0003a0003c0059a0017c0024others(7): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
synonymous_variant | LOW | c.7611T>C | p.Leu2537Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7779/10290 | 7611/9345 | 2537/3114 | chr1 | 214647181 | ||
chr1:214651746
|
T | C | 1 | a0006c0030 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.8020T>C | p.Leu2674Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/20 | 8188/10290 | 8020/9345 | 2674/3114 | chr1 | 214651746 | ||
chr1:214655246
|
C | T | 7 | a0004c0013a0004c0033a0007c0012others(4): Show | 14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
synonymous_variant | LOW | c.8328C>T | p.Asp2776Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/20 | 8496/10290 | 8328/9345 | 2776/3114 | chr1 | 214655246 | ||
chr1:214658968
|
C | T | 3 | a0016c0052a0038c0051a0047c0056 | 3 | HG02055.hp2 HG03041.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.9081C>T | p.Leu3027Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/20 | 9249/10290 | 9081/9345 | 3027/3114 | chr1 | 214658968 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214603264
|
C | G | 31 | a0002c0002t0002a0003c0003t0002a0003c0003t0013others(28): Show | 107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-99C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/20 | 10491 | chr1 | 214603264 | |||||
chr1:214603306
|
C | G | 7 | a0013c0015t0004a0016c0029t0004a0036c0049t0004others(4): Show | 11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-57C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/20 | 10449 | chr1 | 214603306 | |||||
chr1:214663867
|
T | C | 1 | a0002c0002t0005 | 4 | HG00639.hp2 HG02698.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*73T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 73 | chr1 | 214663867 | |||||
chr1:214663910
|
C | T | 1 | a0001c0001t0011 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 116 | chr1 | 214663910 | |||||
chr1:214663928
|
A | G | 1 | a0011c0034t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 134 | chr1 | 214663928 | |||||
chr1:214663956
|
G | C | 1 | a0019c0025t0012 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 162 | chr1 | 214663956 | |||||
chr1:214663993
|
G | A | 5 | a0001c0001t0008a0003c0003t0013a0005c0005t0003others(2): Show | 19 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*199G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 199 | chr1 | 214663993 | |||||
chr1:214664326
|
C | T | 3 | a0018c0020t0006a0028c0040t0010a0043c0043t0006 | 5 | HG02486.hp1 HG03239.hp2 HG03704.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*532C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 532 | chr1 | 214664326 | |||||
chr1:214664331
|
A | G | 1 | a0011c0034t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 537 | chr1 | 214664331 | |||||
chr1:214664380
|
G | A | 1 | a0002c0002t0007 | 2 | HG01433.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 586 | chr1 | 214664380 | |||||
chr1:214664441
|
G | A | 1 | a0003c0003t0013 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*647G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 647 | chr1 | 214664441 | |||||
chr1:214664547
|
A | G | 1 | a0001c0001t0009 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 753 | chr1 | 214664547 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214603487
|
C | G | 44 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(41): Show | 49 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.-42+166C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603487 | ||||||
chr1:214603537
|
T | C | 107 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(104): Show | 118 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.-42+216T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603537 | ||||||
chr1:214603585
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-42+264C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603585 | ||||||
chr1:214603593
|
G | A | 28 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(25): Show | 28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+272G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603593 | ||||||
chr1:214603752
|
T | C | 28 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(25): Show | 28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+431T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603752 | ||||||
chr1:214603823
|
AT | A | 39 | a0001c0001t0001g0076a0001c0001t0001g0078a0004c0013t0002g0031others(36): Show | 39 | HG00642.hp2 HG01106.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-42+513delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214603823 | |||||
chr1:214603823
|
ATT | A | 43 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(40): Show | 48 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.-42+512_-42+513del others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214603823 | |||||
chr1:214603933
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-42+612G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603933 | ||||||
chr1:214603972
|
A | G | 1 | a0025c0026t0002g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-42+651A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603972 | ||||||
chr1:214604073
|
G | T | 3 | a0015c0019t0001g0079a0015c0019t0001g0080a0015c0019t0001g0081 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-42+752G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604073 | ||||||
chr1:214604311
|
T | C | 16 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(13): Show | 21 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42+990T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604311 | ||||||
chr1:214604466
|
T | A | 1 | a0008c0006t0001g0083 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-42+1145T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604466 | ||||||
chr1:214604467
|
C | G | 1 | a0002c0002t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-42+1146C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604467 | ||||||
chr1:214604602
|
T | G | 2 | a0044c0045t0003g0240a0045c0044t0003g0239 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-42+1281T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604602 | ||||||
chr1:214604634
|
T | C | 28 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(25): Show | 28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+1313T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604634 | ||||||
chr1:214604816
|
A | T | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+1495A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604816 | ||||||
chr1:214604864
|
G | A | 11 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(8): Show | 11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-42+1543G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604864 | ||||||
chr1:214605066
|
C | G | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+1745C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605066 | ||||||
chr1:214605101
|
T | A | 44 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(41): Show | 50 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.-42+1780T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605101 | ||||||
chr1:214605441
|
G | GT | 23 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(20): Show | 29 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42+2135dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214605441 | |||||
chr1:214605441
|
GT | G | 9 | a0001c0001t0001g0076a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG01070.hp2 HG01496.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42+2135delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214605441 | |||||
chr1:214605455
|
T | C | 1 | a0034c0054t0002g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42+2134T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605455 | ||||||
chr1:214605457
|
A | T | 3 | a0002c0002t0001g0209a0017c0024t0002g0046a0017c0024t0002g0047 | 3 | HG00558.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+2136A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605457 | ||||||
chr1:214605481
|
T | G | 1 | a0004c0004t0002g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-42+2160T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605481 | ||||||
chr1:214605567
|
G | A | 22 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(19): Show | 28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-42+2246G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605567 | ||||||
chr1:214605585
|
CG | C | 28 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(25): Show | 28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+2269delG | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214605585 | |||||
chr1:214605688
|
C | A | 22 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(19): Show | 28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-42+2367C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605688 | ||||||
chr1:214605804
|
T | C | 44 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(41): Show | 49 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.-42+2483T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605804 | ||||||
chr1:214605809
|
G | C | 1 | a0036c0049t0004g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-42+2488G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605809 | ||||||
chr1:214605865
|
G | A | 1 | a0002c0002t0001g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-42+2544G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605865 | ||||||
chr1:214605897
|
A | G | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-42+2576A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605897 | ||||||
chr1:214605988
|
C | T | 28 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(25): Show | 28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+2667C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605988 | ||||||
chr1:214606004
|
C | T | 27 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(24): Show | 33 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-42+2683C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606004 | ||||||
chr1:214606018
|
C | T | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+2697C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606018 | ||||||
chr1:214606084
|
A | C | 40 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(37): Show | 45 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(42): Show |
intron_variant | MODIFIER | c.-42+2763A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606084 | ||||||
chr1:214606097
|
G | A | 12 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-42+2776G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606097 | ||||||
chr1:214606097
|
G | T | 1 | a0015c0019t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-42+2776G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606097 | ||||||
chr1:214606109
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-42+2788G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606109 | ||||||
chr1:214606133
|
C | G | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+2812C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606133 | ||||||
chr1:214606145
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-42+2824G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606145 | ||||||
chr1:214606273
|
C | T | 1 | a0004c0004t0002g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-42+2952C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606273 | ||||||
chr1:214606276
|
G | T | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+2955G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606276 | ||||||
chr1:214606283
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-42+2962C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606283 | ||||||
chr1:214606286
|
CCCGTTCC others(9): Show |
C | 42 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(39): Show | 53 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.-42+2979_-42+2994d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214606286 | |||||
chr1:214606314
|
C | T | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-42+2993C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606314 | ||||||
chr1:214606371
|
T | A | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+3050T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606371 | ||||||
chr1:214606444
|
T | G | 1 | a0002c0002t0001g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-42+3123T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606444 | ||||||
chr1:214606467
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-42+3146C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606467 | ||||||
chr1:214606665
|
C | T | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-42+3344C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606665 | ||||||
chr1:214606718
|
C | T | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+3397C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606718 | ||||||
chr1:214606832
|
G | A | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+3511G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606832 | ||||||
chr1:214606985
|
C | T | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-42+3664C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606985 | ||||||
chr1:214607018
|
A | T | 1 | a0003c0003t0002g0059 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-42+3697A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607018 | ||||||
chr1:214607050
|
G | A | 1 | a0005c0005t0003g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-42+3729G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607050 | ||||||
chr1:214607178
|
C | G | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-42+3857C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607178 | ||||||
chr1:214607409
|
C | T | 1 | a0038c0051t0001g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-42+4088C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607409 | ||||||
chr1:214607410
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-42+4089G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607410 | ||||||
chr1:214607593
|
G | A | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+4272G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607593 | ||||||
chr1:214607844
|
G | A | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+4523G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607844 | ||||||
chr1:214607921
|
G | A | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+4600G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607921 | ||||||
chr1:214608100
|
G | T | 30 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(27): Show | 30 | HG00642.hp2 HG01109.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-42+4779G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608100 | ||||||
chr1:214608172
|
G | C | 8 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42+4851G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608172 | ||||||
chr1:214608231
|
C | G | 3 | a0018c0020t0006g0213a0018c0020t0006g0214a0018c0020t0006g0215 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-42+4910C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608231 | ||||||
chr1:214608283
|
C | T | 1 | a0032c0041t0001g0204 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-42+4962C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608283 | ||||||
chr1:214608342
|
C | T | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-42+5021C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608342 | ||||||
chr1:214608446
|
A | G | 2 | a0024c0028t0002g0233a0024c0028t0002g0234 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-42+5125A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608446 | ||||||
chr1:214608599
|
C | T | 1 | a0025c0026t0002g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-41-5115C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608599 | ||||||
chr1:214608621
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-41-5093C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608621 | ||||||
chr1:214608628
|
C | T | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41-5086C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608628 | ||||||
chr1:214608786
|
G | A | 55 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(52): Show | 61 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-41-4928G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608786 | ||||||
chr1:214608810
|
A | G | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41-4904A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608810 | ||||||
chr1:214608944
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-41-4770G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608944 | ||||||
chr1:214608985
|
C | T | 2 | a0042c0046t0002g0027a0047c0056t0002g0026 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-41-4729C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608985 | ||||||
chr1:214609028
|
G | T | 1 | a0030c0031t0001g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-41-4686G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609028 | ||||||
chr1:214609097
|
T | C | 103 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(100): Show | 114 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.-41-4617T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609097 | ||||||
chr1:214609122
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-41-4592C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609122 | ||||||
chr1:214609186
|
A | AC | 6 | a0001c0001t0001g0203a0003c0003t0002g0007a0003c0003t0002g0060others(3): Show | 6 | HG00544.hp2 HG02004.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-4526dupC | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214609186 | |||||
chr1:214609563
|
C | T | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-4151C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609563 | ||||||
chr1:214609564
|
C | T | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-4150C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609564 | ||||||
chr1:214609646
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-4068A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609646 | ||||||
chr1:214609656
|
G | T | 15 | a0004c0004t0002g0222a0004c0004t0002g0224a0004c0004t0002g0226others(12): Show | 15 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41-4058G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609656 | ||||||
chr1:214609842
|
C | G | 22 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(19): Show | 28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-41-3872C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609842 | ||||||
chr1:214609991
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-3723T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609991 | ||||||
chr1:214610019
|
C | CT | 9 | a0001c0001t0001g0088a0001c0001t0001g0195a0001c0001t0001g0196others(6): Show | 9 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41-3677dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610019 | |||||
chr1:214610019
|
CT | C | 83 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(80): Show | 90 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-41-3677delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610019 | |||||
chr1:214610019
|
CTT | C | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-41-3678_-41-3677d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610019 | |||||
chr1:214610119
|
A | G | 1 | a0003c0003t0002g0073 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-41-3595A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610119 | ||||||
chr1:214610208
|
C | A | 3 | a0004c0033t0002g0028a0011c0034t0014g0029a0035c0035t0002g0030 | 3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-41-3506C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610208 | ||||||
chr1:214610441
|
A | T | 3 | a0015c0019t0001g0079a0015c0019t0001g0080a0015c0019t0001g0081 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-41-3273A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610441 | ||||||
chr1:214610479
|
AT | A | 52 | a0001c0011t0001g0126a0003c0003t0002g0003a0003c0003t0002g0005others(49): Show | 58 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-41-3219delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610479 | |||||
chr1:214610484
|
T | G | 23 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(20): Show | 23 | HG01109.hp1 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41-3230T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610484 | ||||||
chr1:214610523
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-3191T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610523 | ||||||
chr1:214610551
|
G | A | 3 | a0015c0019t0001g0079a0015c0019t0001g0080a0015c0019t0001g0081 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-41-3163G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610551 | ||||||
chr1:214610751
|
A | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-2963A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610751 | ||||||
chr1:214610771
|
G | A | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-41-2943G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610771 | ||||||
chr1:214610838
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-2876T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610838 | ||||||
chr1:214610848
|
A | G | 24 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(21): Show | 30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.-41-2866A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610848 | ||||||
chr1:214610919
|
A | T | 3 | a0018c0020t0006g0213a0018c0020t0006g0214a0018c0020t0006g0215 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-41-2795A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610919 | ||||||
chr1:214611022
|
A | G | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-41-2692A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611022 | ||||||
chr1:214611137
|
TG | T | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41-2576delG | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611137 | ||||||
chr1:214611580
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-41-2134G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611580 | ||||||
chr1:214611678
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-41-2036T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611678 | ||||||
chr1:214611889
|
A | G | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-41-1825A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611889 | ||||||
chr1:214611893
|
G | T | 11 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(8): Show | 11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41-1821G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611893 | ||||||
chr1:214611955
|
A | G | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41-1759A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611955 | ||||||
chr1:214612117
|
A | G | 1 | a0005c0005t0003g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-41-1597A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612117 | ||||||
chr1:214612300
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-41-1414C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612300 | ||||||
chr1:214612592
|
C | T | 1 | a0040c0047t0002g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-41-1122C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612592 | ||||||
chr1:214612691
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-41-1023C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612691 | ||||||
chr1:214613094
|
T | C | 107 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(104): Show | 118 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.-41-620T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613094 | ||||||
chr1:214613292
|
A | C | 160 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(157): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-41-422A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613292 | ||||||
chr1:214613318
|
T | C | 107 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(104): Show | 118 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.-41-396T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613318 | ||||||
chr1:214613402
|
C | A | 3 | a0007c0012t0001g0010a0007c0012t0001g0085a0007c0012t0001g0128 | 4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-312C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613402 | ||||||
chr1:214613457
|
T | C | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-41-257T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613457 | ||||||
chr1:214613639
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-41-75A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613639 | ||||||
chr1:214613971
|
G | C | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162+55G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214613971 | ||||||
chr1:214614087
|
A | G | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.162+171A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614087 | ||||||
chr1:214614108
|
C | CT | 60 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(57): Show | 66 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.162+205dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 214614108 | |||||
chr1:214614108
|
C | CTT | 15 | a0004c0004t0002g0221a0004c0013t0002g0031a0004c0013t0002g0032others(12): Show | 15 | HG00642.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.162+204_162+205dup others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 214614108 | |||||
chr1:214614184
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.162+268G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614184 | ||||||
chr1:214614200
|
A | G | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.162+284A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614200 | ||||||
chr1:214614216
|
A | G | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+300A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614216 | ||||||
chr1:214614217
|
C | T | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162+301C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614217 | ||||||
chr1:214614591
|
A | T | 1 | a0015c0019t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163-241A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614591 | ||||||
chr1:214615084
|
C | T | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.359+56C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615084 | ||||||
chr1:214615121
|
T | C | 1 | a0015c0019t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359+93T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615121 | ||||||
chr1:214615157
|
C | T | 8 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0187others(5): Show | 8 | HG00544.hp2 HG02040.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.359+129C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615157 | ||||||
chr1:214615240
|
C | T | 3 | a0004c0033t0002g0028a0011c0034t0014g0029a0035c0035t0002g0030 | 3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.359+212C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615240 | ||||||
chr1:214615336
|
A | G | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.359+308A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615336 | ||||||
chr1:214615341
|
T | G | 1 | a0034c0054t0002g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+313T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615341 | ||||||
chr1:214615389
|
T | G | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.359+361T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615389 | ||||||
chr1:214615496
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0193a0022c0027t0001g0131others(1): Show | 4 | HG01081.hp2 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+468G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615496 | ||||||
chr1:214615696
|
T | C | 1 | a0034c0054t0002g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+668T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615696 | ||||||
chr1:214615994
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.359+966C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615994 | ||||||
chr1:214615997
|
A | G | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.359+969A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615997 | ||||||
chr1:214616032
|
T | C | 104 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(101): Show | 115 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.359+1004T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616032 | ||||||
chr1:214616058
|
C | T | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.359+1030C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616058 | ||||||
chr1:214616189
|
T | C | 1 | a0002c0002t0001g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.359+1161T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616189 | ||||||
chr1:214616294
|
A | T | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.359+1266A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616294 | ||||||
chr1:214616561
|
A | G | 34 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(31): Show | 34 | HG00642.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.359+1533A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616561 | ||||||
chr1:214616819
|
CTTCTTTC others(25): Show |
C | 1 | a0049c0060t0004g0054 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.360-1752_360-1721d others(34): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | |||||
chr1:214616819
|
CTTCTTTC others(33): Show |
C | 1 | a0013c0015t0004g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.360-1752_360-1713d others(42): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | |||||
chr1:214616819
|
CTTCTTTC others(37): Show |
C | 2 | a0013c0015t0004g0051a0013c0015t0004g0052 | 2 | HG01109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.360-1752_360-1709d others(46): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | |||||
chr1:214616819
|
CTTCTTTC others(41): Show |
C | 1 | a0013c0015t0004g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360-1752_360-1705d others(50): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | |||||
chr1:214616827
|
CTTCCTTC others(12): Show |
C | 1 | a0035c0035t0002g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.360-1742_360-1724d others(21): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616827 | |||||
chr1:214616831
|
CTTCCTCT others(16): Show |
C | 1 | a0012c0014t0002g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.360-1738_360-1716d others(25): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616831 | |||||
chr1:214616834
|
CCTCTTTC others(1): Show |
C | 3 | a0004c0013t0002g0035a0012c0014t0002g0020a0012c0014t0002g0022 | 3 | HG01106.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.360-1738_360-1731d others(10): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | ||||||
chr1:214616834
|
CCTCTTTC others(5): Show |
C | 2 | a0004c0033t0002g0028a0011c0034t0014g0029 | 2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.360-1738_360-1727d others(14): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | ||||||
chr1:214616834
|
CCTCTTTC others(9): Show |
C | 1 | a0004c0013t0002g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.360-1738_360-1723d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | ||||||
chr1:214616834
|
CCTCTTTC others(13): Show |
C | 4 | a0004c0013t0002g0031a0004c0013t0002g0032a0012c0014t0002g0021others(1): Show | 4 | HG02559.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.360-1738_360-1719d others(22): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | ||||||
chr1:214616834
|
CCTCTTTC others(15): Show |
C | 1 | a0018c0020t0006g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360-1736_360-1715d others(24): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616834 | |||||
chr1:214616835
|
C | CTCTTTCT others(5): Show |
1 | a0022c0027t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.360-1661_360-1650d others(14): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
C | CTCTTTCT others(9): Show |
1 | a0001c0017t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.360-1665_360-1650d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTT | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0001t0001g0092others(9): Show | 14 | HG00673.hp2 HG01258.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.360-1653_360-1650d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(1): Show |
C | 19 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0086others(16): Show | 20 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-1657_360-1650d others(10): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(5): Show |
C | 35 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0161others(32): Show | 42 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.360-1661_360-1650d others(14): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(8): Show |
C | 1 | a0002c0002t0002g0243 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.360-1736_360-1722d others(17): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(9): Show |
C | 49 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0147others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.360-1665_360-1650d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(13): Show |
C | 35 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0078others(32): Show | 37 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.360-1669_360-1650d others(22): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(17): Show |
C | 31 | a0001c0001t0001g0088a0001c0001t0001g0135a0001c0001t0001g0137others(28): Show | 34 | HG00140.hp2 HG01074.hp1 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.360-1673_360-1650d others(26): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(21): Show |
C | 22 | a0001c0001t0001g0093a0001c0001t0001g0127a0001c0001t0001g0134others(19): Show | 25 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.360-1677_360-1650d others(30): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(25): Show |
C | 6 | a0002c0002t0001g0209a0003c0003t0002g0005a0005c0005t0003g0249others(3): Show | 8 | HG00558.hp2 HG02622.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-1681_360-1650d others(34): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(29): Show |
C | 3 | a0003c0003t0002g0062a0005c0005t0003g0248a0005c0005t0003g0252 | 3 | HG00408.hp2 HG01346.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.360-1685_360-1650d others(38): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(33): Show |
C | 4 | a0005c0005t0003g0002a0005c0005t0003g0245a0005c0005t0003g0247others(1): Show | 8 | HG03704.hp2 NA18943.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.360-1689_360-1650d others(42): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616835
|
CTCTTTCT others(37): Show |
C | 1 | a0005c0005t0003g0016 | 2 | HG01496.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.360-1693_360-1650d others(46): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | |||||
chr1:214616841
|
CTTTCTTT others(10): Show |
C | 1 | a0002c0002t0005g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360-1729_360-1713d others(19): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616841 | |||||
chr1:214616850
|
T | C | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-1723T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616850 | ||||||
chr1:214616858
|
T | C | 1 | a0018c0020t0006g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360-1715T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616858 | ||||||
chr1:214616862
|
TTTCTTTC others(12): Show |
T | 1 | a0014c0016t0001g0183 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.360-1708_360-1690d others(21): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616862 | |||||
chr1:214616873
|
C | A | 2 | a0016c0029t0004g0018a0036c0049t0004g0049 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.360-1700C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616873 | ||||||
chr1:214616877
|
C | A | 1 | a0016c0029t0004g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.360-1696C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616877 | ||||||
chr1:214616888
|
TCTTTCTT others(44): Show |
T | 1 | a0004c0004t0002g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.360-1683_360-1633d others(53): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616888 | |||||
chr1:214616892
|
TCTTTCTT others(40): Show |
T | 1 | a0004c0004t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.360-1679_360-1633d others(49): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616892 | |||||
chr1:214616893
|
CT | C | 4 | a0004c0004t0002g0217a0004c0004t0002g0218a0004c0004t0002g0222others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1677delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616893 | |||||
chr1:214616896
|
TCTTTCTT others(36): Show |
T | 2 | a0024c0028t0002g0233a0024c0028t0002g0234 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.360-1675_360-1633d others(45): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616896 | |||||
chr1:214616900
|
TCTTTCTT others(32): Show |
T | 1 | a0004c0004t0002g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.360-1671_360-1633d others(41): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616900 | |||||
chr1:214616904
|
TCTTTCTT others(28): Show |
T | 4 | a0004c0004t0002g0217a0004c0004t0002g0218a0004c0004t0002g0222others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1667_360-1633d others(37): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616904 | |||||
chr1:214616905
|
CTTTCTTT others(6): Show |
C | 1 | a0004c0004t0002g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.360-1665_360-1653d others(15): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616905 | |||||
chr1:214616918
|
TTTC | T | 5 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-1649_360-1647d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616918 | |||||
chr1:214616934
|
ACCCTCCC others(1): Show |
A | 13 | a0004c0004t0002g0212a0004c0004t0002g0219a0004c0004t0002g0220others(10): Show | 13 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.360-1630_360-1623d others(10): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616934 | |||||
chr1:214616942
|
T | A | 9 | a0004c0004t0002g0216a0004c0004t0002g0217a0004c0004t0002g0218others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.360-1631T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616942 | ||||||
chr1:214616964
|
C | T | 2 | a0044c0045t0003g0240a0045c0044t0003g0239 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.360-1609C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616964 | ||||||
chr1:214617000
|
C | CTCTT | 6 | a0002c0002t0001g0109a0004c0013t0002g0031a0004c0013t0002g0032others(3): Show | 6 | HG02109.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.360-1557_360-1554d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214617000 | |||||
chr1:214617291
|
G | A | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.360-1282G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617291 | ||||||
chr1:214617345
|
G | A | 1 | a0018c0020t0006g0214 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.360-1228G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617345 | ||||||
chr1:214617363
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0208a0033c0036t0001g0094 | 3 | HG02523.hp2 NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.360-1210C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617363 | ||||||
chr1:214617453
|
G | A | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.360-1120G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617453 | ||||||
chr1:214617713
|
C | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.360-860C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617713 | ||||||
chr1:214617733
|
A | G | 1 | a0019c0025t0002g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.360-840A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617733 | ||||||
chr1:214617782
|
A | G | 1 | a0004c0004t0002g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.360-791A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617782 | ||||||
chr1:214617798
|
C | T | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.360-775C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617798 | ||||||
chr1:214617949
|
T | C | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.360-624T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617949 | ||||||
chr1:214618093
|
C | T | 1 | a0022c0027t0001g0132 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.360-480C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618093 | ||||||
chr1:214618146
|
C | T | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-427C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618146 | ||||||
chr1:214618190
|
C | T | 2 | a0018c0020t0006g0214a0018c0020t0006g0215 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.360-383C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618190 | ||||||
chr1:214618269
|
C | G | 11 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(8): Show | 11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-304C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618269 | ||||||
chr1:214618441
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.360-132A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618441 | ||||||
chr1:214618511
|
A | G | 1 | a0004c0013t0002g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.360-62A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618511 | ||||||
chr1:214618552
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.360-21T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618552 | ||||||
chr1:214618906
|
G | T | 22 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(19): Show | 28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.481+212G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 4/19 | chr1 | 214618906 | ||||||
chr1:214618937
|
A | G | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.482-192A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 4/19 | chr1 | 214618937 | ||||||
chr1:214619006
|
C | G | 23 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(20): Show | 29 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.482-123C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 4/19 | chr1 | 214619006 | ||||||
chr1:214619260
|
T | C | 1 | a0009c0010t0001g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.573+40T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619260 | ||||||
chr1:214619330
|
G | T | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.573+110G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619330 | ||||||
chr1:214619422
|
A | G | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+202A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619422 | ||||||
chr1:214619483
|
A | G | 1 | a0034c0054t0002g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.573+263A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619483 | ||||||
chr1:214619535
|
C | T | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+315C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619535 | ||||||
chr1:214620040
|
T | G | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.574-615T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620040 | ||||||
chr1:214620043
|
C | CAAA | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-606_574-604dup others(3): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 214620043 | |||||
chr1:214620302
|
C | T | 8 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-353C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620302 | ||||||
chr1:214620470
|
G | A | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.574-185G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620470 | ||||||
chr1:214620513
|
A | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.574-142A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620513 | ||||||
chr1:214620525
|
G | A | 6 | a0009c0010t0001g0139a0009c0010t0001g0143a0009c0010t0001g0144others(3): Show | 6 | HG02055.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-130G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620525 | ||||||
chr1:214621054
|
A | G | 1 | a0004c0013t0002g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.865+108A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621054 | ||||||
chr1:214621153
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.865+207A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621153 | ||||||
chr1:214621183
|
C | G | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.865+237C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621183 | ||||||
chr1:214621213
|
T | A | 49 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(46): Show | 55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.865+267T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621213 | ||||||
chr1:214621219
|
G | A | 1 | a0050c0061t0004g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.865+273G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621219 | ||||||
chr1:214621252
|
G | A | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.865+306G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621252 | ||||||
chr1:214621284
|
A | C | 1 | a0002c0002t0001g0117 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.865+338A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621284 | ||||||
chr1:214621368
|
A | G | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.865+422A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621368 | ||||||
chr1:214621464
|
G | A | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.865+518G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621464 | ||||||
chr1:214621897
|
T | C | 1 | a0003c0003t0002g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.866-182T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621897 | ||||||
chr1:214621964
|
G | T | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.866-115G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621964 | ||||||
chr1:214622040
|
A | G | 1 | a0009c0010t0001g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.866-39A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214622040 | ||||||
chr1:214622296
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1068+15G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622296 | ||||||
chr1:214622451
|
C | T | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+170C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622451 | ||||||
chr1:214622492
|
T | C | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+211T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622492 | ||||||
chr1:214622556
|
T | C | 49 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(46): Show | 55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1068+275T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622556 | ||||||
chr1:214622654
|
GGATCGTA others(83): Show |
G | 95 | a0001c0001t0001g0142a0003c0003t0002g0003a0003c0003t0002g0005others(92): Show | 107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.1068+553_1068+642d others(92): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214622654 | |||||
chr1:214622654
|
GGATCGTA others(173): Show |
G | 16 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(13): Show | 16 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1068+463_1068+642d others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214622654 | |||||
chr1:214622749
|
G | A | 1 | a0018c0020t0006g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1068+468G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622749 | ||||||
chr1:214622852
|
G | A | 2 | a0002c0002t0001g0091a0002c0002t0001g0110 | 2 | HG00140.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1068+571G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622852 | ||||||
chr1:214622868
|
A | G | 3 | a0018c0020t0006g0213a0018c0020t0006g0214a0018c0020t0006g0215 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1068+587A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622868 | ||||||
chr1:214622883
|
G | C | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+602G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622883 | ||||||
chr1:214622902
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1068+621C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622902 | ||||||
chr1:214622917
|
G | A | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+636G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622917 | ||||||
chr1:214622934
|
G | A | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+653G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622934 | ||||||
chr1:214622941
|
T | C | 49 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(46): Show | 55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1068+660T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622941 | ||||||
chr1:214622963
|
A | G | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+682A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622963 | ||||||
chr1:214622967
|
T | G | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+686T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622967 | ||||||
chr1:214622979
|
A | G | 1 | a0011c0034t0014g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1068+698A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622979 | ||||||
chr1:214622986
|
C | T | 1 | a0007c0009t0001g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1068+705C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622986 | ||||||
chr1:214623054
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0140 | 2 | HG01978.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1068+773T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623054 | ||||||
chr1:214623056
|
C | T | 1 | a0004c0013t0002g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1068+775C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623056 | ||||||
chr1:214623103
|
C | T | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1068+822C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623103 | ||||||
chr1:214623147
|
G | T | 1 | a0003c0003t0002g0061 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1068+866G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623147 | ||||||
chr1:214623170
|
C | G | 1 | a0005c0005t0003g0250 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1068+889C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623170 | ||||||
chr1:214623189
|
T | C | 202 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0076others(199): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1068+908T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623189 | ||||||
chr1:214623285
|
A | G | 3 | a0005c0005t0003g0016a0005c0005t0003g0248a0005c0005t0003g0252 | 4 | HG01346.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068+1004A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623285 | ||||||
chr1:214623495
|
C | T | 9 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(6): Show | 9 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+1214C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623495 | ||||||
chr1:214623544
|
TTTG | T | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+1281_1068+128 others(7): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214623544 | |||||
chr1:214623617
|
T | G | 22 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(19): Show | 28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1068+1336T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623617 | ||||||
chr1:214623681
|
A | G | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+1400A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623681 | ||||||
chr1:214623713
|
G | A | 1 | a0012c0014t0002g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1068+1432G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623713 | ||||||
chr1:214623841
|
A | G | 7 | a0002c0002t0001g0004a0010c0008t0001g0004a0010c0008t0001g0077others(4): Show | 9 | NA18941.hp1 NA18943.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1068+1560A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623841 | ||||||
chr1:214624002
|
A | C | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068+1721A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624002 | ||||||
chr1:214624010
|
ATTTTAAG others(19): Show |
A | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068+1730_1068+175 others(30): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624010 | ||||||
chr1:214624169
|
A | AT | 14 | a0004c0004t0002g0226a0005c0005t0003g0002a0005c0005t0003g0016others(11): Show | 19 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1068+1897dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214624169 | |||||
chr1:214624242
|
T | C | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1068+1961T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624242 | ||||||
chr1:214624249
|
C | A | 1 | a0002c0002t0001g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1068+1968C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624249 | ||||||
chr1:214624365
|
A | G | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1068+2084A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624365 | ||||||
chr1:214624370
|
A | C | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1068+2089A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624370 | ||||||
chr1:214624434
|
C | G | 1 | a0003c0003t0002g0062 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1068+2153C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624434 | ||||||
chr1:214624531
|
T | C | 1 | a0004c0033t0002g0028 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1068+2250T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624531 | ||||||
chr1:214624588
|
T | G | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+2307T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624588 | ||||||
chr1:214624715
|
AT | A | 8 | a0001c0011t0001g0126a0001c0011t0001g0160a0003c0003t0002g0063others(5): Show | 8 | HG02273.hp2 HG03139.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+2445delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214624715 | |||||
chr1:214624776
|
C | T | 1 | a0032c0041t0001g0204 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1068+2495C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624776 | ||||||
chr1:214624823
|
G | A | 1 | a0001c0017t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1068+2542G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624823 | ||||||
chr1:214624879
|
G | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1068+2598G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624879 | ||||||
chr1:214624910
|
C | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1068+2629C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624910 | ||||||
chr1:214624978
|
A | G | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+2697A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624978 | ||||||
chr1:214625143
|
A | G | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+2862A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625143 | ||||||
chr1:214625189
|
G | C | 1 | a0022c0027t0001g0132 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1068+2908G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625189 | ||||||
chr1:214625237
|
C | T | 53 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(50): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1068+2956C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625237 | ||||||
chr1:214625334
|
C | A | 14 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(11): Show | 14 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1068+3053C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625334 | ||||||
chr1:214625459
|
A | G | 163 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(160): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1068+3178A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625459 | ||||||
chr1:214625493
|
T | G | 1 | a0025c0026t0002g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1068+3212T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625493 | ||||||
chr1:214625511
|
G | A | 2 | a0016c0029t0004g0017a0016c0029t0004g0018 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1068+3230G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625511 | ||||||
chr1:214625512
|
C | T | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+3231C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625512 | ||||||
chr1:214625551
|
A | G | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+3270A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625551 | ||||||
chr1:214625586
|
G | C | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+3305G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625586 | ||||||
chr1:214625650
|
T | C | 1 | a0002c0002t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1068+3369T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625650 | ||||||
chr1:214625677
|
T | G | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1069-3369T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625677 | ||||||
chr1:214625688
|
T | A | 1 | a0002c0002t0001g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1069-3358T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625688 | ||||||
chr1:214625901
|
T | C | 2 | a0013c0015t0004g0050a0013c0015t0004g0051 | 2 | HG01109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1069-3145T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625901 | ||||||
chr1:214625963
|
A | G | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-3083A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625963 | ||||||
chr1:214625995
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-3051A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625995 | ||||||
chr1:214626027
|
A | G | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1069-3019A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626027 | ||||||
chr1:214626035
|
A | C | 5 | a0016c0029t0004g0017a0016c0029t0004g0018a0036c0049t0004g0049others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-3011A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626035 | ||||||
chr1:214626156
|
G | C | 1 | a0006c0007t0002g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1069-2890G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626156 | ||||||
chr1:214626427
|
T | A | 2 | a0019c0025t0002g0236a0019c0025t0012g0237 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1069-2619T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626427 | ||||||
chr1:214626551
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-2495C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626551 | ||||||
chr1:214626785
|
C | T | 8 | a0006c0007t0002g0038a0006c0007t0002g0040a0006c0007t0002g0041others(5): Show | 8 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-2261C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626785 | ||||||
chr1:214626804
|
T | C | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-2242T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626804 | ||||||
chr1:214626854
|
G | A | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1069-2192G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626854 | ||||||
chr1:214626864
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1069-2182T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626864 | ||||||
chr1:214626921
|
A | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-2125A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626921 | ||||||
chr1:214627045
|
T | C | 27 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(24): Show | 33 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1069-2001T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627045 | ||||||
chr1:214627129
|
A | T | 160 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(157): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1069-1917A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627129 | ||||||
chr1:214627203
|
G | A | 1 | a0002c0002t0007g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1069-1843G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627203 | ||||||
chr1:214627204
|
C | T | 2 | a0011c0018t0002g0225a0011c0018t0002g0238 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1069-1842C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627204 | ||||||
chr1:214627250
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-1796A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627250 | ||||||
chr1:214627257
|
C | T | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1069-1789C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627257 | ||||||
chr1:214627261
|
G | A | 8 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-1785G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627261 | ||||||
chr1:214627289
|
G | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-1757G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627289 | ||||||
chr1:214627369
|
C | CT | 142 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0076others(139): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1069-1656dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214627369 | |||||
chr1:214627369
|
C | CTT | 47 | a0001c0001t0001g0198a0001c0001t0001g0201a0003c0003t0002g0074others(44): Show | 52 | HG00642.hp2 HG01109.hp1 HG01346.hp2 others(49): Show |
intron_variant | MODIFIER | c.1069-1657_1069-165 others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214627369 | |||||
chr1:214627369
|
C | CTTT | 7 | a0004c0013t0002g0035a0005c0005t0003g0247a0017c0024t0002g0046others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-1658_1069-165 others(7): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214627369 | |||||
chr1:214627476
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-1570T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627476 | ||||||
chr1:214627619
|
G | A | 8 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-1427G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627619 | ||||||
chr1:214627806
|
C | G | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-1240C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627806 | ||||||
chr1:214627811
|
G | A | 2 | a0006c0007t0002g0036a0006c0007t0002g0045 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1069-1235G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627811 | ||||||
chr1:214627871
|
T | C | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1069-1175T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627871 | ||||||
chr1:214628295
|
G | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-751G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628295 | ||||||
chr1:214628299
|
C | T | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1069-747C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628299 | ||||||
chr1:214628477
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1069-569C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628477 | ||||||
chr1:214628569
|
C | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-477C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628569 | ||||||
chr1:214628591
|
A | T | 42 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(39): Show | 48 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-455A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628591 | ||||||
chr1:214628601
|
C | T | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-445C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628601 | ||||||
chr1:214628669
|
G | T | 1 | a0001c0001t0001g0015 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1069-377G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628669 | ||||||
chr1:214628677
|
A | T | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1069-369A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628677 | ||||||
chr1:214628917
|
C | A | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1069-129C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628917 | ||||||
chr1:214628956
|
C | T | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1069-90C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628956 | ||||||
chr1:214628981
|
C | G | 1 | a0018c0020t0006g0214 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1069-65C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628981 | ||||||
chr1:214629344
|
T | C | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+173T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629344 | ||||||
chr1:214629353
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1194+182A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629353 | ||||||
chr1:214629460
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+289T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629460 | ||||||
chr1:214629481
|
G | A | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+310G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629481 | ||||||
chr1:214629514
|
T | A | 2 | a0006c0007t0002g0036a0006c0007t0002g0045 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1194+343T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629514 | ||||||
chr1:214629516
|
A | C | 2 | a0017c0024t0002g0046a0017c0024t0002g0047 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1194+345A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629516 | ||||||
chr1:214629518
|
A | T | 5 | a0016c0029t0004g0017a0016c0029t0004g0018a0036c0049t0004g0049others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+347A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629518 | ||||||
chr1:214629558
|
A | AT | 9 | a0001c0001t0001g0206a0013c0015t0004g0050a0013c0015t0004g0051others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1194+398dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 214629558 | |||||
chr1:214629558
|
A | ATATTTTT others(7): Show |
2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+388_1194+389i others(16): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 214629558 | |||||
chr1:214629568
|
T | C | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1194+397T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629568 | ||||||
chr1:214629582
|
C | T | 2 | a0044c0045t0003g0240a0045c0044t0003g0239 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1194+411C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629582 | ||||||
chr1:214629608
|
A | G | 2 | a0023c0023t0001g0084a0023c0023t0001g0191 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1194+437A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629608 | ||||||
chr1:214629748
|
T | C | 49 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(46): Show | 55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1194+577T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629748 | ||||||
chr1:214629771
|
C | T | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1194+600C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629771 | ||||||
chr1:214629793
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+622T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629793 | ||||||
chr1:214629924
|
T | A | 23 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(20): Show | 29 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1195-610T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629924 | ||||||
chr1:214629965
|
T | G | 4 | a0005c0005t0003g0002a0005c0005t0003g0245a0005c0005t0003g0247others(1): Show | 8 | HG01993.hp1 NA18943.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195-569T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629965 | ||||||
chr1:214630134
|
AAAG | A | 15 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1195-399_1195-397d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630134 | ||||||
chr1:214630178
|
A | G | 1 | a0034c0054t0002g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1195-356A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630178 | ||||||
chr1:214630202
|
T | C | 2 | a0019c0025t0002g0236a0019c0025t0012g0237 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1195-332T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630202 | ||||||
chr1:214630306
|
T | C | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1195-228T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630306 | ||||||
chr1:214630404
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1195-130G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630404 | ||||||
chr1:214630416
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1195-118A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630416 | ||||||
chr1:214630502
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1195-32T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630502 | ||||||
chr1:214630698
|
C | A | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1323+36C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214630698 | ||||||
chr1:214630766
|
G | A | 3 | a0018c0020t0006g0213a0018c0020t0006g0214a0018c0020t0006g0215 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1323+104G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214630766 | ||||||
chr1:214630941
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+279T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214630941 | ||||||
chr1:214631010
|
A | G | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1323+348A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631010 | ||||||
chr1:214631066
|
A | G | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1323+404A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631066 | ||||||
chr1:214631076
|
G | A | 2 | a0019c0025t0002g0236a0019c0025t0012g0237 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1323+414G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631076 | ||||||
chr1:214631297
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+635C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631297 | ||||||
chr1:214631298
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+636A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631298 | ||||||
chr1:214631299
|
C | G | 1 | a0006c0007t0002g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1323+637C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631299 | ||||||
chr1:214631305
|
T | A | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+643T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631305 | ||||||
chr1:214631390
|
CTT | C | 7 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323+730_1323+731d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr1 | 214631390 | |||||
chr1:214631571
|
C | T | 3 | a0007c0012t0001g0010a0007c0012t0001g0085a0007c0012t0001g0128 | 4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+909C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631571 | ||||||
chr1:214631635
|
G | A | 2 | a0023c0023t0001g0084a0023c0023t0001g0191 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1324-845G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631635 | ||||||
chr1:214631644
|
C | T | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1324-836C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631644 | ||||||
chr1:214631719
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1324-761C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631719 | ||||||
chr1:214631817
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0194 | 3 | HG00408.hp1 HG00423.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1324-663C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631817 | ||||||
chr1:214631899
|
C | T | 1 | a0035c0035t0002g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1324-581C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631899 | ||||||
chr1:214631913
|
G | A | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1324-567G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631913 | ||||||
chr1:214631922
|
G | A | 4 | a0015c0019t0001g0079a0015c0019t0001g0080a0015c0019t0001g0081others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-558G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631922 | ||||||
chr1:214632113
|
A | C | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1324-367A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632113 | ||||||
chr1:214632140
|
G | GA | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-336dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr1 | 214632140 | |||||
chr1:214632159
|
C | T | 8 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-321C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632159 | ||||||
chr1:214632189
|
G | A | 11 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(8): Show | 11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1324-291G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632189 | ||||||
chr1:214632287
|
A | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1324-193A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632287 | ||||||
chr1:214632290
|
C | T | 3 | a0004c0033t0002g0028a0011c0034t0014g0029a0035c0035t0002g0030 | 3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1324-190C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632290 | ||||||
chr1:214632442
|
A | G | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-38A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632442 | ||||||
chr1:214632729
|
GAAGT | G | 24 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(21): Show | 30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1446+133_1446+136d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214632729 | |||||
chr1:214632940
|
G | A | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+338G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214632940 | ||||||
chr1:214633062
|
TAAAC | T | 7 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1446+464_1446+467d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214633062 | |||||
chr1:214633078
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+476C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633078 | ||||||
chr1:214633123
|
C | A | 4 | a0006c0007t0002g0042a0006c0007t0002g0044a0006c0030t0002g0037others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+521C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633123 | ||||||
chr1:214633133
|
T | C | 53 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(50): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1446+531T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633133 | ||||||
chr1:214633188
|
G | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+586G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633188 | ||||||
chr1:214633222
|
T | C | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+620T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633222 | ||||||
chr1:214633388
|
A | G | 1 | a0004c0004t0002g0230 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1446+786A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633388 | ||||||
chr1:214633564
|
A | G | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1446+962A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633564 | ||||||
chr1:214633611
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0193a0022c0027t0001g0131others(1): Show | 4 | HG01081.hp2 HG01261.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1009C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633611 | ||||||
chr1:214633715
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1446+1113G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633715 | ||||||
chr1:214633734
|
A | AC | 84 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(81): Show | 90 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1446+1133dupC | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214633734 | |||||
chr1:214633782
|
G | A | 14 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1446+1180G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633782 | ||||||
chr1:214633934
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1446+1332C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633934 | ||||||
chr1:214634057
|
C | T | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1455C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634057 | ||||||
chr1:214634083
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+1481C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634083 | ||||||
chr1:214634100
|
G | A | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1446+1498G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634100 | ||||||
chr1:214634130
|
C | A | 53 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(50): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1446+1528C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634130 | ||||||
chr1:214634172
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+1570C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634172 | ||||||
chr1:214634231
|
G | C | 4 | a0015c0019t0001g0079a0015c0019t0001g0080a0015c0019t0001g0081others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1629G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634231 | ||||||
chr1:214634327
|
G | A | 15 | a0004c0004t0002g0222a0004c0004t0002g0224a0004c0004t0002g0226others(12): Show | 15 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+1725G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634327 | ||||||
chr1:214634366
|
C | G | 24 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(21): Show | 30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1446+1764C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634366 | ||||||
chr1:214634457
|
C | T | 1 | a0005c0005t0003g0250 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1446+1855C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634457 | ||||||
chr1:214634458
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(248): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1446+1856A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634458 | ||||||
chr1:214634756
|
A | G | 5 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(2): Show | 5 | HG02717.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+2154A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634756 | ||||||
chr1:214634777
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+2175A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634777 | ||||||
chr1:214634951
|
T | C | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+2349T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634951 | ||||||
chr1:214635064
|
G | A | 3 | a0002c0002t0005g0095a0002c0002t0005g0106a0002c0002t0005g0118 | 3 | HG00639.hp2 HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1446+2462G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635064 | ||||||
chr1:214635079
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1446+2477C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635079 | ||||||
chr1:214635210
|
T | A | 1 | a0011c0018t0002g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1446+2608T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635210 | ||||||
chr1:214635238
|
A | G | 7 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1447-2628A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635238 | ||||||
chr1:214635680
|
C | T | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1447-2186C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635680 | ||||||
chr1:214635770
|
T | A | 14 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1447-2096T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635770 | ||||||
chr1:214635807
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1447-2059T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635807 | ||||||
chr1:214635869
|
G | C | 1 | a0017c0055t0002g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1447-1997G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635869 | ||||||
chr1:214635991
|
T | A | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1447-1875T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635991 | ||||||
chr1:214636087
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1447-1779C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636087 | ||||||
chr1:214636156
|
T | C | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1710T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636156 | ||||||
chr1:214636173
|
C | T | 1 | a0002c0002t0001g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1447-1693C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636173 | ||||||
chr1:214636221
|
A | G | 3 | a0007c0012t0001g0010a0007c0012t0001g0085a0007c0012t0001g0128 | 4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-1645A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636221 | ||||||
chr1:214636684
|
C | T | 1 | a0003c0059t0002g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1447-1182C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636684 | ||||||
chr1:214636764
|
C | T | 2 | a0013c0015t0004g0050a0013c0015t0004g0051 | 2 | HG01109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1447-1102C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636764 | ||||||
chr1:214636839
|
C | T | 1 | a0004c0013t0002g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1447-1027C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636839 | ||||||
chr1:214636938
|
G | C | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1447-928G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636938 | ||||||
chr1:214637191
|
C | T | 1 | a0016c0052t0001g0169 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-675C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637191 | ||||||
chr1:214637324
|
T | C | 31 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(28): Show | 31 | HG00642.hp2 HG01109.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1447-542T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637324 | ||||||
chr1:214637425
|
T | G | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1447-441T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637425 | ||||||
chr1:214637465
|
A | AT | 34 | a0002c0002t0001g0210a0005c0005t0003g0002a0005c0005t0003g0016others(31): Show | 39 | HG01070.hp1 HG01106.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1447-386dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214637465 | |||||
chr1:214637511
|
G | A | 1 | a0002c0002t0001g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1447-355G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637511 | ||||||
chr1:214637534
|
A | G | 4 | a0012c0014t0002g0020a0012c0014t0002g0021a0012c0014t0002g0022others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-332A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637534 | ||||||
chr1:214637607
|
G | A | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1447-259G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637607 | ||||||
chr1:214637739
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0011g0200 | 2 | HG02040.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1447-127G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637739 | ||||||
chr1:214637831
|
G | A | 24 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(21): Show | 30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1447-35G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637831 | ||||||
chr1:214638049
|
C | T | 1 | a0002c0002t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1582+48C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638049 | ||||||
chr1:214638181
|
G | C | 4 | a0005c0005t0003g0002a0005c0005t0003g0245a0005c0005t0003g0247others(1): Show | 8 | HG01993.hp1 NA18943.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1582+180G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638181 | ||||||
chr1:214638502
|
C | G | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1582+501C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638502 | ||||||
chr1:214638519
|
C | G | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1582+518C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638519 | ||||||
chr1:214638605
|
A | G | 50 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(47): Show | 56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582+604A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638605 | ||||||
chr1:214638688
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1582+687C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638688 | ||||||
chr1:214638697
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0153 | 3 | HG02723.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1582+696G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638697 | ||||||
chr1:214638742
|
C | A | 2 | a0019c0025t0002g0236a0019c0025t0012g0237 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1582+741C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638742 | ||||||
chr1:214638782
|
C | T | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1582+781C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638782 | ||||||
chr1:214638783
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1582+782G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638783 | ||||||
chr1:214638873
|
G | T | 1 | a0004c0013t0002g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1582+872G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638873 | ||||||
chr1:214638921
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1582+920C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638921 | ||||||
chr1:214638939
|
G | A | 50 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(47): Show | 56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582+938G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638939 | ||||||
chr1:214639246
|
T | A | 1 | a0023c0023t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1583-675T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639246 | ||||||
chr1:214639567
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01070.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1583-354A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639567 | ||||||
chr1:214639633
|
A | G | 3 | a0011c0018t0002g0225a0011c0018t0002g0232a0011c0018t0002g0238 | 3 | HG02630.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1583-288A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639633 | ||||||
chr1:214639718
|
A | G | 165 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(162): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1583-203A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639718 | ||||||
chr1:214639729
|
T | C | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1583-192T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639729 | ||||||
chr1:214643372
|
G | A | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+48G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643372 | ||||||
chr1:214643375
|
C | T | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.4986+51C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643375 | ||||||
chr1:214643499
|
A | T | 2 | a0016c0029t0004g0017a0016c0029t0004g0018 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4986+175A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643499 | ||||||
chr1:214643601
|
G | A | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4986+277G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643601 | ||||||
chr1:214643688
|
T | TATG | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+365_4986+367d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr1 | 214643688 | |||||
chr1:214643740
|
A | G | 3 | a0007c0012t0001g0010a0007c0012t0001g0085a0007c0012t0001g0128 | 4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4986+416A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643740 | ||||||
chr1:214643765
|
C | G | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+441C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643765 | ||||||
chr1:214643791
|
T | A | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4986+467T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643791 | ||||||
chr1:214643852
|
G | A | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+528G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643852 | ||||||
chr1:214643888
|
T | A | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+564T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643888 | ||||||
chr1:214644021
|
T | C | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4987-536T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644021 | ||||||
chr1:214644111
|
G | A | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4987-446G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644111 | ||||||
chr1:214644131
|
G | A | 3 | a0018c0020t0006g0213a0018c0020t0006g0214a0018c0020t0006g0215 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4987-426G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644131 | ||||||
chr1:214644228
|
A | G | 32 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(29): Show | 38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4987-329A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644228 | ||||||
chr1:214644378
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0153 | 3 | HG02723.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4987-179C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644378 | ||||||
chr1:214644513
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4987-44T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644513 | ||||||
chr1:214647590
|
A | G | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.7830+190A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214647590 | ||||||
chr1:214647657
|
G | A | 1 | a0011c0018t0002g0225 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7830+257G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214647657 | ||||||
chr1:214647877
|
A | G | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.7830+477A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214647877 | ||||||
chr1:214648029
|
G | A | 1 | a0004c0004t0002g0230 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7830+629G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648029 | ||||||
chr1:214648048
|
G | C | 2 | a0021c0022t0001g0115a0030c0031t0001g0202 | 2 | HG01515.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.7831-627G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648048 | ||||||
chr1:214648072
|
A | C | 36 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(33): Show | 42 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.7831-603A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648072 | ||||||
chr1:214648113
|
C | G | 48 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(45): Show | 54 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.7831-562C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648113 | ||||||
chr1:214648166
|
G | T | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.7831-509G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648166 | ||||||
chr1:214648287
|
T | C | 1 | a0008c0006t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.7831-388T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648287 | ||||||
chr1:214648318
|
A | G | 6 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(3): Show | 6 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.7831-357A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648318 | ||||||
chr1:214648337
|
G | C | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.7831-338G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648337 | ||||||
chr1:214648356
|
TA | T | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.7831-317delA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr1 | 214648356 | |||||
chr1:214648472
|
A | C | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.7831-203A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648472 | ||||||
chr1:214648546
|
C | T | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7831-129C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648546 | ||||||
chr1:214648616
|
G | A | 25 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(22): Show | 31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.7831-59G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648616 | ||||||
chr1:214648916
|
T | C | 1 | a0008c0006t0001g0083 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7983+89T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214648916 | ||||||
chr1:214649098
|
C | T | 10 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.7983+271C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649098 | ||||||
chr1:214649106
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.7983+279C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649106 | ||||||
chr1:214649170
|
G | A | 1 | a0003c0003t0002g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7983+343G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649170 | ||||||
chr1:214649316
|
G | A | 6 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(3): Show | 6 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.7983+489G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649316 | ||||||
chr1:214649326
|
C | G | 21 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(18): Show | 21 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.7983+499C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649326 | ||||||
chr1:214649493
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.7983+666T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649493 | ||||||
chr1:214649559
|
G | T | 13 | a0006c0007t0002g0036a0006c0007t0002g0038a0006c0007t0002g0040others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.7983+732G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649559 | ||||||
chr1:214650072
|
T | A | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7983+1245T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650072 | ||||||
chr1:214650111
|
A | G | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.7983+1284A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650111 | ||||||
chr1:214650145
|
T | C | 9 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(6): Show | 9 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.7983+1318T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650145 | ||||||
chr1:214650201
|
G | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7983+1374G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650201 | ||||||
chr1:214650203
|
T | G | 96 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(93): Show | 107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.7983+1376T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650203 | ||||||
chr1:214650358
|
G | C | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.7984-1352G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650358 | ||||||
chr1:214650461
|
C | T | 2 | a0001c0001t0001g0203a0032c0041t0001g0204 | 2 | HG00544.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7984-1249C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650461 | ||||||
chr1:214650505
|
A | G | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7984-1205A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650505 | ||||||
chr1:214650550
|
A | G | 22 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.7984-1160A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650550 | ||||||
chr1:214650579
|
C | T | 2 | a0019c0025t0002g0236a0019c0025t0012g0237 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.7984-1131C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650579 | ||||||
chr1:214650667
|
C | T | 34 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(31): Show | 40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.7984-1043C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650667 | ||||||
chr1:214650738
|
C | CA | 20 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(17): Show | 20 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.7984-965dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 214650738 | |||||
chr1:214650774
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0141 | 3 | HG02698.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.7984-936A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650774 | ||||||
chr1:214650814
|
A | G | 9 | a0017c0024t0002g0046a0017c0024t0002g0047a0018c0020t0006g0213others(6): Show | 9 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.7984-896A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650814 | ||||||
chr1:214650999
|
G | C | 1 | a0035c0035t0002g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7984-711G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650999 | ||||||
chr1:214651050
|
C | A | 52 | a0003c0003t0002g0003a0003c0003t0002g0005a0003c0003t0002g0007others(49): Show | 63 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.7984-660C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651050 | ||||||
chr1:214651088
|
G | T | 1 | a0003c0003t0002g0065 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.7984-622G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651088 | ||||||
chr1:214651193
|
A | G | 13 | a0005c0005t0003g0002a0005c0005t0003g0016a0005c0005t0003g0244others(10): Show | 18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.7984-517A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651193 | ||||||
chr1:214651326
|
C | T | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7984-384C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651326 | ||||||
chr1:214651334
|
A | G | 4 | a0006c0007t0002g0038a0006c0007t0002g0040a0006c0007t0002g0041others(1): Show | 4 | HG02109.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.7984-376A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651334 | ||||||
chr1:214651464
|
A | G | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7984-246A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651464 | ||||||
chr1:214651476
|
G | A | 2 | a0004c0033t0002g0028a0011c0034t0014g0029 | 2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.7984-234G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651476 | ||||||
chr1:214651496
|
G | A | 1 | a0024c0028t0002g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7984-214G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651496 | ||||||
chr1:214651561
|
A | G | 2 | a0004c0033t0002g0028a0011c0034t0014g0029 | 2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.7984-149A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651561 | ||||||
chr1:214651637
|
T | C | 1 | a0025c0026t0002g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7984-73T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651637 | ||||||
chr1:214651946
|
C | CT | 7 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.8160+72dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214651946 | |||||
chr1:214651946
|
C | CTT | 54 | a0004c0004t0002g0222a0004c0004t0002g0224a0004c0004t0002g0226others(51): Show | 59 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(56): Show |
intron_variant | MODIFIER | c.8160+71_8160+72dup others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214651946 | |||||
chr1:214652068
|
A | ATTTTT | 16 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(13): Show | 16 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.8160+196_8160+200d others(7): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | |||||
chr1:214652068
|
A | ATTTTTTT | 8 | a0006c0007t0002g0038a0006c0007t0002g0040a0006c0007t0002g0041others(5): Show | 8 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.8160+194_8160+200d others(9): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | |||||
chr1:214652068
|
AT | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0176a0002c0002t0001g0004others(57): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.8160+200delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | |||||
chr1:214652068
|
ATT | A | 34 | a0002c0002t0001g0091a0004c0013t0002g0031a0004c0013t0002g0032others(31): Show | 39 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.8160+199_8160+200d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | |||||
chr1:214652121
|
C | T | 2 | a0025c0026t0002g0024a0025c0026t0002g0048 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8160+235C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652121 | ||||||
chr1:214652146
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.8160+260C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652146 | ||||||
chr1:214652185
|
G | A | 13 | a0003c0003t0002g0066a0005c0005t0003g0002a0005c0005t0003g0016others(10): Show | 18 | HG01074.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8160+299G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652185 | ||||||
chr1:214652211
|
A | G | 1 | a0003c0003t0013g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.8160+325A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652211 | ||||||
chr1:214652222
|
T | A | 1 | a0037c0050t0004g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8160+336T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652222 | ||||||
chr1:214652229
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0002c0002t0001g0097 | 3 | HG01943.hp1 NA18612.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.8160+343G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652229 | ||||||
chr1:214652233
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0009g0194 | 2 | HG00408.hp1 HG00423.hp2 |
intron_variant | MODIFIER | c.8160+347C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652233 | ||||||
chr1:214652234
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0009g0194 | 2 | HG00408.hp1 HG00423.hp2 |
intron_variant | MODIFIER | c.8160+348A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652234 | ||||||
chr1:214652236
|
T | C | 8 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0196others(5): Show | 8 | HG00408.hp1 HG00423.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.8160+350T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652236 | ||||||
chr1:214652237
|
G | A | 1 | a0003c0059t0002g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.8160+351G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652237 | ||||||
chr1:214652242
|
A | G | 1 | a0004c0004t0002g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8160+356A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652242 | ||||||
chr1:214652267
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(194): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.8160+381T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652267 | ||||||
chr1:214652294
|
C | T | 1 | a0002c0032t0001g0119 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.8160+408C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652294 | ||||||
chr1:214652326
|
C | T | 68 | a0001c0001t0001g0166a0002c0002t0001g0004a0002c0002t0001g0009others(65): Show | 71 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.8160+440C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652326 | ||||||
chr1:214652380
|
A | G | 5 | a0011c0034t0014g0029a0017c0024t0002g0046a0017c0024t0002g0047others(2): Show | 5 | HG01891.hp2 HG02257.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8161-448A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652380 | ||||||
chr1:214652408
|
C | T | 13 | a0001c0001t0008g0197a0005c0005t0003g0002a0005c0005t0003g0016others(10): Show | 18 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8161-420C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652408 | ||||||
chr1:214652411
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.8161-417G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652411 | ||||||
chr1:214652444
|
CT | C | 124 | a0001c0001t0001g0093a0001c0001t0001g0153a0001c0001t0001g0161others(121): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.8161-367delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652444 | |||||
chr1:214652444
|
CTT | C | 8 | a0002c0002t0001g0111a0002c0002t0001g0210a0002c0002t0002g0241others(5): Show | 8 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.8161-368_8161-367d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652444 | |||||
chr1:214652455
|
T | C | 1 | a0002c0002t0001g0188 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8161-373T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652455 | ||||||
chr1:214652471
|
C | T | 72 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(69): Show | 75 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.8161-357C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652471 | ||||||
chr1:214652505
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(206): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.8161-323A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652505 | ||||||
chr1:214652529
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(234): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.8161-299T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652529 | ||||||
chr1:214652589
|
G | A | 3 | a0005c0005t0003g0016a0005c0005t0003g0248a0005c0005t0003g0252 | 4 | HG01346.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.8161-239G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652589 | ||||||
chr1:214652632
|
CAG | C | 73 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(70): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.8161-195_8161-194d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652632 | ||||||
chr1:214652742
|
T | C | 14 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.8161-86T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652742 | ||||||
chr1:214653021
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(123): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.8322+32G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653021 | ||||||
chr1:214653028
|
T | G | 1 | a0016c0052t0001g0169 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8322+39T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653028 | ||||||
chr1:214653127
|
C | A | 15 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(12): Show | 16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+138C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653127 | ||||||
chr1:214653249
|
T | C | 3 | a0003c0003t0002g0060a0003c0003t0002g0064a0003c0003t0002g0065 | 3 | HG02135.hp2 NA18966.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.8322+260T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653249 | ||||||
chr1:214653309
|
G | C | 6 | a0019c0025t0002g0236a0019c0025t0012g0237a0024c0028t0002g0233others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.8322+320G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653309 | ||||||
chr1:214653311
|
C | T | 15 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(12): Show | 16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+322C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653311 | ||||||
chr1:214653365
|
C | T | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8322+376C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653365 | ||||||
chr1:214653423
|
C | T | 7 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.8322+434C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653423 | ||||||
chr1:214653434
|
TCTC | T | 5 | a0009c0010t0001g0139a0009c0010t0001g0143a0009c0010t0001g0159others(2): Show | 5 | HG02055.hp1 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.8322+449_8322+451d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214653434 | |||||
chr1:214653466
|
ACT | A | 5 | a0009c0010t0001g0139a0009c0010t0001g0143a0009c0010t0001g0159others(2): Show | 5 | HG02055.hp1 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.8322+478_8322+479d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653466 | ||||||
chr1:214653467
|
CT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(190): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.8322+493delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214653467 | |||||
chr1:214653467
|
CTTT | C | 15 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(12): Show | 16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+491_8322+493d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214653467 | |||||
chr1:214653482
|
T | A | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8322+493T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653482 | ||||||
chr1:214653614
|
G | A | 15 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(12): Show | 16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+625G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653614 | ||||||
chr1:214653645
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(198): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.8322+656A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653645 | ||||||
chr1:214653696
|
G | A | 1 | a0043c0043t0006g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.8322+707G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653696 | ||||||
chr1:214653719
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(123): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.8322+730G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653719 | ||||||
chr1:214653723
|
C | T | 15 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(12): Show | 16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+734C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653723 | ||||||
chr1:214653934
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(213): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.8322+945A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653934 | ||||||
chr1:214654070
|
T | C | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8322+1081T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654070 | ||||||
chr1:214654177
|
A | G | 1 | a0021c0022t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.8323-1064A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654177 | ||||||
chr1:214654188
|
C | T | 1 | a0004c0033t0002g0028 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.8323-1053C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654188 | ||||||
chr1:214654360
|
G | A | 61 | a0002c0002t0001g0004a0002c0002t0001g0009a0002c0002t0001g0082others(58): Show | 63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.8323-881G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654360 | ||||||
chr1:214654362
|
C | T | 1 | a0040c0047t0002g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.8323-879C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654362 | ||||||
chr1:214654404
|
C | G | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8323-837C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654404 | ||||||
chr1:214654441
|
C | T | 28 | a0004c0004t0002g0222a0004c0004t0002g0224a0004c0004t0002g0226others(25): Show | 29 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.8323-800C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654441 | ||||||
chr1:214654516
|
A | G | 13 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(10): Show | 14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-725A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654516 | ||||||
chr1:214654518
|
G | C | 2 | a0024c0028t0002g0233a0024c0028t0002g0234 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8323-723G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654518 | ||||||
chr1:214654960
|
T | C | 13 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(10): Show | 14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-281T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654960 | ||||||
chr1:214654965
|
T | TA | 13 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(10): Show | 14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-273dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214654965 | |||||
chr1:214655007
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(190): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.8323-234T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214655007 | ||||||
chr1:214655015
|
A | G | 9 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(6): Show | 9 | HG00642.hp2 HG02145.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.8323-226A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214655015 | ||||||
chr1:214655090
|
C | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(153): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.8323-151C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214655090 | ||||||
chr1:214655178
|
A | AT | 13 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(10): Show | 14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-58dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214655178 | |||||
chr1:214655469
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(190): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.8485+66A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655469 | ||||||
chr1:214655545
|
A | G | 12 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(9): Show | 13 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.8485+142A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655545 | ||||||
chr1:214655624
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(190): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.8485+221A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655624 | ||||||
chr1:214655667
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(164): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.8485+264G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655667 | ||||||
chr1:214655694
|
G | A | 2 | a0017c0055t0002g0019a0032c0041t0001g0204 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.8485+291G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655694 | ||||||
chr1:214655748
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(164): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.8485+345A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655748 | ||||||
chr1:214655752
|
G | A | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8485+349G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655752 | ||||||
chr1:214655769
|
T | C | 1 | a0005c0005t0003g0250 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.8485+366T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655769 | ||||||
chr1:214655851
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(159): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.8485+448A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655851 | ||||||
chr1:214655866
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(164): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.8485+463T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655866 | ||||||
chr1:214655877
|
C | T | 1 | a0004c0013t0002g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8485+474C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655877 | ||||||
chr1:214656028
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8485+625C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656028 | ||||||
chr1:214656056
|
G | C | 15 | a0004c0004t0002g0222a0004c0004t0002g0224a0004c0004t0002g0226others(12): Show | 15 | HG02145.hp2 HG02572.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.8485+653G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656056 | ||||||
chr1:214656235
|
G | A | 2 | a0004c0004t0002g0235a0007c0009t0001g0158 | 2 | HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8486-698G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656235 | ||||||
chr1:214656268
|
G | A | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8486-665G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656268 | ||||||
chr1:214656305
|
A | G | 1 | a0037c0050t0004g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8486-628A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656305 | ||||||
chr1:214656342
|
T | A | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8486-591T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656342 | ||||||
chr1:214656448
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(149): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.8486-485T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656448 | ||||||
chr1:214656465
|
A | G | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.8486-468A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656465 | ||||||
chr1:214656573
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(149): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.8486-360T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656573 | ||||||
chr1:214656630
|
A | T | 1 | a0010c0008t0001g0100 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.8486-303A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656630 | ||||||
chr1:214656657
|
G | A | 2 | a0016c0052t0001g0169a0038c0051t0001g0205 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.8486-276G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656657 | ||||||
chr1:214656682
|
G | A | 1 | a0002c0002t0001g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.8486-251G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656682 | ||||||
chr1:214656799
|
A | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(149): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.8486-134A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656799 | ||||||
chr1:214656822
|
T | TA | 12 | a0004c0013t0002g0031a0004c0013t0002g0032a0004c0013t0002g0033others(9): Show | 12 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.8486-100dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 214656822 | |||||
chr1:214656822
|
TA | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(152): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.8486-100delA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 214656822 | |||||
chr1:214656863
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.8486-70G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656863 | ||||||
chr1:214656872
|
T | C | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8486-61T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656872 | ||||||
chr1:214657565
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(150): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.8962+156A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657565 | ||||||
chr1:214657662
|
T | C | 3 | a0007c0012t0001g0010a0007c0012t0001g0085a0007c0012t0001g0128 | 4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.8962+253T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657662 | ||||||
chr1:214657706
|
G | A | 13 | a0001c0001t0008g0197a0005c0005t0003g0002a0005c0005t0003g0016others(10): Show | 18 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8962+297G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657706 | ||||||
chr1:214657739
|
A | G | 13 | a0001c0001t0008g0197a0005c0005t0003g0002a0005c0005t0003g0016others(10): Show | 18 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8962+330A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657739 | ||||||
chr1:214657741
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(120): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.8962+332C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657741 | ||||||
chr1:214657892
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.8962+483G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657892 | ||||||
chr1:214657918
|
A | T | 3 | a0015c0019t0001g0079a0015c0019t0001g0080a0034c0054t0002g0211 | 3 | HG02615.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8962+509A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657918 | ||||||
chr1:214657944
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(147): Show | 172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.8962+535A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657944 | ||||||
chr1:214658062
|
C | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0076others(25): Show | 29 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.8962+653C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658062 | ||||||
chr1:214658086
|
G | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(147): Show | 172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.8962+677G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658086 | ||||||
chr1:214658186
|
GAA | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(148): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.8963-658_8963-657d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 214658186 | |||||
chr1:214658334
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0156 | 2 | NA18950.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.8963-516C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658334 | ||||||
chr1:214658336
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(151): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.8963-514T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658336 | ||||||
chr1:214658487
|
T | A | 1 | a0004c0013t0002g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8963-363T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658487 | ||||||
chr1:214658556
|
A | G | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8963-294A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658556 | ||||||
chr1:214658586
|
A | T | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8963-264A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658586 | ||||||
chr1:214659168
|
G | A | 2 | a0019c0025t0002g0236a0019c0025t0012g0237 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.9141+140G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659168 | ||||||
chr1:214659204
|
A | G | 1 | a0011c0034t0014g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9141+176A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659204 | ||||||
chr1:214659446
|
TA | T | 33 | a0001c0001t0008g0197a0004c0013t0002g0031a0004c0013t0002g0032others(30): Show | 38 | HG00423.hp1 HG01109.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.9141+431delA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 214659446 | |||||
chr1:214659522
|
G | T | 1 | a0037c0050t0004g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.9141+494G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659522 | ||||||
chr1:214659833
|
C | G | 1 | a0050c0061t0004g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.9141+805C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659833 | ||||||
chr1:214659940
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.9141+912G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659940 | ||||||
chr1:214659945
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9141+917C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659945 | ||||||
chr1:214660082
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(124): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.9141+1054G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660082 | ||||||
chr1:214660127
|
A | G | 7 | a0004c0004t0002g0212a0004c0004t0002g0216a0004c0004t0002g0217others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.9141+1099A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660127 | ||||||
chr1:214660191
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(150): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.9141+1163A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660191 | ||||||
chr1:214660365
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9141+1337C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660365 | ||||||
chr1:214660379
|
C | T | 26 | a0001c0001t0008g0197a0003c0003t0013g0068a0005c0005t0003g0002others(23): Show | 31 | HG00423.hp1 HG01109.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.9141+1351C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660379 | ||||||
chr1:214660517
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9141+1489C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660517 | ||||||
chr1:214660755
|
A | G | 3 | a0015c0019t0001g0079a0015c0019t0001g0080a0034c0054t0002g0211 | 3 | HG02615.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.9141+1727A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660755 | ||||||
chr1:214660846
|
G | A | 2 | a0017c0055t0002g0019a0032c0041t0001g0204 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9141+1818G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660846 | ||||||
chr1:214661017
|
C | T | 2 | a0012c0014t0002g0021a0012c0014t0002g0022 | 2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.9141+1989C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661017 | ||||||
chr1:214661048
|
C | T | 6 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(3): Show | 6 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.9141+2020C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661048 | ||||||
chr1:214661055
|
C | T | 1 | a0011c0034t0014g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9141+2027C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661055 | ||||||
chr1:214661247
|
A | G | 1 | a0011c0034t0014g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9141+2219A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661247 | ||||||
chr1:214661313
|
A | G | 2 | a0017c0055t0002g0019a0032c0041t0001g0204 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9142-2278A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661313 | ||||||
chr1:214661452
|
A | C | 1 | a0039c0053t0004g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9142-2139A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661452 | ||||||
chr1:214661505
|
C | T | 1 | a0006c0007t0002g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9142-2086C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661505 | ||||||
chr1:214661604
|
C | T | 1 | a0011c0034t0014g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9142-1987C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661604 | ||||||
chr1:214661755
|
G | T | 1 | a0019c0025t0002g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.9142-1836G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661755 | ||||||
chr1:214661833
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.9142-1758T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661833 | ||||||
chr1:214661874
|
CT | C | 35 | a0001c0001t0001g0092a0001c0001t0001g0151a0001c0001t0001g0152others(32): Show | 40 | HG00323.hp2 HG00423.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.9142-1706delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 214661874 | |||||
chr1:214662311
|
G | A | 1 | a0002c0002t0001g0113 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.9142-1280G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662311 | ||||||
chr1:214662412
|
G | T | 1 | a0002c0002t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9142-1179G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662412 | ||||||
chr1:214662515
|
T | C | 1 | a0047c0056t0002g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.9142-1076T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662515 | ||||||
chr1:214662655
|
T | C | 2 | a0044c0045t0003g0240a0045c0044t0003g0239 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.9142-936T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662655 | ||||||
chr1:214662719
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.9142-872A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662719 | ||||||
chr1:214662873
|
G | A | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9142-718G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662873 | ||||||
chr1:214662878
|
C | T | 1 | a0046c0058t0002g0025 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9142-713C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662878 | ||||||
chr1:214662883
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.9142-708G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662883 | ||||||
chr1:214662925
|
G | A | 11 | a0013c0015t0004g0050a0013c0015t0004g0051a0013c0015t0004g0052others(8): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.9142-666G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662925 | ||||||
chr1:214663035
|
G | A | 1 | a0042c0046t0002g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9142-556G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663035 | ||||||
chr1:214663113
|
A | G | 14 | a0001c0001t0008g0197a0003c0003t0013g0068a0005c0005t0003g0002others(11): Show | 19 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.9142-478A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663113 | ||||||
chr1:214663157
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.9142-434T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663157 | ||||||
chr1:214663525
|
C | T | 2 | a0004c0004t0002g0224a0004c0004t0002g0227 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.9142-66C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663525 | ||||||
chr1:214663575
|
G | T | 1 | a0004c0013t0002g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9142-16G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663575 |