geneid | 51131 |
---|---|
ensemblid | ENSG00000136147.18 |
hgncid | 17024 |
symbol | PHF11 |
name | PHD finger protein 11 |
refseq_nuc | NM_001040443.3 |
refseq_prot | NP_001035533.1 |
ensembl_nuc | ENST00000378319.8 |
ensembl_prot | ENSP00000367570.3 |
mane_status | MANE Select |
chr | chr13 |
start | 49495953 |
end | 49528976 |
strand | + |
ver | v1.2 |
region | chr13:49495953-49528976 |
region5000 | chr13:49490953-49533976 |
regionname0 | PHF11_chr13_49495953_49528976 |
regionname5000 | PHF11_chr13_49490953_49533976 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 331 | 405 | 84 | 76 | 187 | 14 | 42 | 141 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0002 | 0/0 | 324 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0003 | 0/0 | 331 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0004 | 0/0 | 331 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0005 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 996 | 327 | 77 | 48 | 161 | 8 | 32 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0002 | 1/0 | 996 | 74 | 7 | 26 | 24 | 6 | 10 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0003 | 0/0 | 975 | 5 | 5 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0004 | 0/0 | 996 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0005 | 0/0 | 996 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0006 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0007 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
c0008 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 361 | 185 | 58 | 37 | 61 | 6 | 22 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
t0002 | 0/1 | 361 | 179 | 32 | 36 | 89 | 7 | 14 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
t0003 | 0/0 | 364 | 49 | 1 | 3 | 38 | 1 | 6 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
t0004 | 0/0 | 361 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 0 | 2 | 14 | 0 | 3 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0002 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0003 | 0/0 | 6 | 0 | 1 | 2 | 1 | 2 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0029 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 996 | 327 | 77 | 48 | 161 | 8 | 32 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0002 | 1/0 | 996 | 74 | 7 | 26 | 24 | 6 | 10 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0004 | 0/0 | 996 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0005 | 0/0 | 996 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0002c0003 | 0/0 | 975 | 5 | 5 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0003c0006 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0004c0008 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0005c0007 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1356 | 107 | 44 | 15 | 36 | 0 | 12 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0001t0002 | 0/1 | 1356 | 170 | 31 | 30 | 87 | 7 | 14 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0001t0003 | 0/0 | 1359 | 49 | 1 | 3 | 38 | 1 | 6 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0001t0004 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0002t0001 | 1/0 | 1356 | 69 | 6 | 22 | 24 | 6 | 10 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0002t0002 | 0/0 | 1356 | 5 | 1 | 4 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0004t0002 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0001c0005t0002 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0002c0003t0001 | 0/0 | 1335 | 5 | 5 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0003c0006t0001 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0004c0008t0001 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
a0005c0007t0001 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | copy fasta | chr13 | 49490953 | 49533976 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0001 | 0/0 | 19 | 0 | 2 | 14 | 0 | 3 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0029 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0003 | 0/0 | 6 | 0 | 1 | 2 | 1 | 2 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0004t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0005t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0001c0005t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0002c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0002c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0002c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0003c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0003c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0004c0008t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
a0005c0007t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0176 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0081 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0331 | EUR | FIN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0319 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0318 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01069 | hp1 | a0001 | c0004 | t0002 | g0008 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01071 | hp1 | a0001 | c0004 | t0002 | g0008 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0329 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0333 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0334 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0076 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0330 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02145 | hp1 | a0002 | c0003 | t0001 | g0041 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0284 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02572 | hp2 | a0005 | c0007 | t0001 | g0066 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0283 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02717 | hp1 | a0003 | c0006 | t0001 | g0070 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03041 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03139 | hp1 | a0003 | c0006 | t0001 | g0069 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0313 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18966 | hp1 | a0001 | c0005 | t0002 | g0162 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18971 | hp1 | a0004 | c0008 | t0001 | g0305 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19030 | hp2 | a0002 | c0003 | t0001 | g0065 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19086 | hp1 | a0001 | c0005 | t0002 | g0178 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ASW | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ASW | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | GIH | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | GIH | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0332 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02109 | hp2 | a0002 | c0003 | t0001 | g0067 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0321 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA21309 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0029 | REF | REF | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0080 | REF | REF | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49496005
|
GCCCAGGC others(14): Show |
G | 1 | a0002 | 5 | HG02109.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
conservative_inframe_deletion | MODERATE | c.7_27delCAGGCGTCGCC others(10): Show |
p.Gln3_Pro9del | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | 56/1356 | 7/996 | 3/331 | INFO_REALIGN_3_PRIME | chr13 | 49496005 | |
chr13:49496062
|
C | G | 1 | a0003 | 2 | HG02717.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.61C>G | p.Arg21Gly | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | 110/1356 | 61/996 | 21/331 | chr13 | 49496062 | ||
chr13:49496071
|
C | G | 1 | a0004 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.70C>G | p.Gln24Glu | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | 119/1356 | 70/996 | 24/331 | chr13 | 49496071 | ||
chr13:49528658
|
C | A | 2 | a0002a0005 | 6 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.989C>A | p.Ser330Tyr | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 1038/1356 | 989/996 | 330/331 | chr13 | 49528658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49506711
|
A | G | 7 | a0001c0001a0001c0004a0001c0005others(4): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
synonymous_variant | LOW | c.171A>G | p.Leu57Leu | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/10 | 220/1356 | 171/996 | 57/331 | chr13 | 49506711 | ||
chr13:49518110
|
C | T | 1 | a0001c0005 | 2 | NA18966.hp1 NA19086.hp1 |
synonymous_variant | LOW | c.417C>T | p.Asp139Asp | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/10 | 466/1356 | 417/996 | 139/331 | chr13 | 49518110 | ||
chr13:49518113
|
C | T | 1 | a0001c0004 | 2 | HG01069.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.420C>T | p.Asp140Asp | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/10 | 469/1356 | 420/996 | 140/331 | chr13 | 49518113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49495984
|
C | T | 1 | a0001c0001t0004 | 1 | NA19240.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | chr13 | 49495984 | ||||||
chr13:49528674
|
G | A | 4 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(1): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 9 | chr13 | 49528674 | |||||
chr13:49528856
|
T | C | 4 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(1): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 191 | chr13 | 49528856 | |||||
chr13:49528946
|
C | CTCT | 1 | a0001c0001t0003 | 49 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*283_*285dupCTT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 286 | INFO_REALIGN_3_PRIME | chr13 | 49528946 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:49496108
|
GGGGC | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(246): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.94+33_94+36delCGGG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496108 | |||||
chr13:49496108
|
GGGGCGGG others(9): Show |
G | 1 | a0001c0001t0001g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94+21_94+36delCGGG others(12): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496108 | |||||
chr13:49496147
|
G | T | 3 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336 | 3 | HG01517.hp2 HG01981.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.94+52G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496147 | ||||||
chr13:49496280
|
G | A | 1 | a0002c0003t0001g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+185G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496280 | ||||||
chr13:49496286
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.94+191G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496286 | ||||||
chr13:49496390
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+295A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496390 | ||||||
chr13:49496465
|
G | A | 1 | a0001c0001t0002g0022 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.94+370G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496465 | ||||||
chr13:49496470
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.94+375G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496470 | ||||||
chr13:49496509
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+414A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496509 | ||||||
chr13:49496612
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+517G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496612 | ||||||
chr13:49496830
|
C | CT | 121 | a0001c0001t0001g0024a0001c0001t0001g0117a0001c0001t0001g0136others(118): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.94+756dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
C | CTT | 13 | a0001c0001t0001g0045a0001c0001t0001g0226a0001c0001t0001g0227others(10): Show | 13 | HG00544.hp1 HG00544.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+755_94+756dupTT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
C | CTTT | 16 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0238others(13): Show | 18 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+754_94+756dupTT others(1): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
C | CTTTT | 36 | a0001c0001t0001g0113a0001c0001t0001g0252a0001c0001t0002g0272others(33): Show | 41 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.94+753_94+756dupTT others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
C | CTTTTT | 42 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0114others(39): Show | 57 | HG00408.hp1 HG00642.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.94+752_94+756dupTT others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
C | CTTTTTT | 12 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(9): Show | 13 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+751_94+756dupTT others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
C | CTTTTTTT | 7 | a0001c0002t0001g0012a0001c0002t0001g0328a0001c0002t0001g0329others(4): Show | 9 | HG00280.hp1 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+750_94+756dupTT others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496830
|
CT | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 27 | HG01109.hp1 HG01257.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+756delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | |||||
chr13:49496926
|
C | T | 108 | a0001c0001t0001g0045a0001c0001t0001g0159a0001c0001t0001g0163others(105): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.94+831C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496926 | ||||||
chr13:49496973
|
A | G | 14 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(11): Show | 14 | HG00438.hp1 HG02074.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+878A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496973 | ||||||
chr13:49497218
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.94+1123G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49497218 | ||||||
chr13:49497571
|
T | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(251): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.94+1476T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49497571 | ||||||
chr13:49497801
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+1706T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49497801 | ||||||
chr13:49498109
|
A | G | 18 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0118others(15): Show | 20 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+2014A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498109 | ||||||
chr13:49498273
|
C | A | 1 | a0001c0001t0002g0203 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.94+2178C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498273 | ||||||
chr13:49498293
|
T | C | 17 | a0001c0002t0001g0010a0001c0002t0001g0012a0001c0002t0001g0040others(14): Show | 22 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+2198T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498293 | ||||||
chr13:49498386
|
AATCATTC others(63): Show |
A | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 44 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.94+2321_94+2390del others(70): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49498386 | |||||
chr13:49498491
|
G | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0120others(12): Show | 17 | HG00621.hp1 HG02165.hp1 HG03490.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+2396G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498491 | ||||||
chr13:49498495
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG01109.hp2 HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.94+2400A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498495 | ||||||
chr13:49498735
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0337 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.94+2640A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498735 | ||||||
chr13:49498839
|
T | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0286 | 3 | HG02056.hp2 HG02135.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.94+2744T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498839 | ||||||
chr13:49498870
|
A | T | 3 | a0001c0001t0002g0005a0001c0001t0002g0316a0001c0001t0002g0327 | 6 | HG01952.hp1 HG01978.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+2775A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498870 | ||||||
chr13:49499223
|
T | G | 7 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0148others(4): Show | 9 | HG01257.hp1 HG01258.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+3128T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499223 | ||||||
chr13:49499282
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+3187G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499282 | ||||||
chr13:49499343
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+3248C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499343 | ||||||
chr13:49499427
|
C | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(251): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.94+3332C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499427 | ||||||
chr13:49499467
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.94+3372T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499467 | ||||||
chr13:49499633
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+3538G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499633 | ||||||
chr13:49499933
|
C | A | 1 | a0001c0001t0002g0213 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.94+3838C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499933 | ||||||
chr13:49499968
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+3873G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499968 | ||||||
chr13:49500014
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94+3919G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500014 | ||||||
chr13:49500521
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 5 | HG02451.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+4426G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500521 | ||||||
chr13:49500546
|
C | T | 2 | a0001c0001t0001g0104a0001c0002t0001g0105 | 2 | HG02056.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.94+4451C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500546 | ||||||
chr13:49500616
|
A | G | 277 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.94+4521A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500616 | ||||||
chr13:49500620
|
A | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.94+4525A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500620 | ||||||
chr13:49500726
|
ACAG | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0203a0001c0001t0002g0212 | 3 | HG00099.hp1 HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.94+4635_94+4637del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49500726 | |||||
chr13:49500782
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+4687G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500782 | ||||||
chr13:49500914
|
C | T | 3 | a0001c0001t0002g0031a0001c0001t0002g0201a0001c0001t0002g0202 | 4 | HG00639.hp1 HG02055.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+4819C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500914 | ||||||
chr13:49500971
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4876C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500971 | ||||||
chr13:49500995
|
C | CT | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0337 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+4904dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49500995 | |||||
chr13:49501000
|
G | GT | 30 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0288others(27): Show | 33 | HG01123.hp1 HG01358.hp2 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+4920dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | |||||
chr13:49501000
|
G | GTT | 29 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0114others(26): Show | 38 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.94+4919_94+4920dup others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | |||||
chr13:49501000
|
G | GTTT | 15 | a0001c0001t0001g0042a0001c0001t0001g0307a0001c0001t0001g0308others(12): Show | 18 | HG00597.hp2 HG00642.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+4918_94+4920dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | |||||
chr13:49501000
|
G | GTTTT | 7 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01074.hp1 HG01433.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4917_94+4920dup others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | |||||
chr13:49501000
|
G | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.94+4905G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501000 | ||||||
chr13:49501001
|
TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0001g0147 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.94+4918_94+4933del others(16): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501001 | |||||
chr13:49501003
|
T | G | 6 | a0001c0002t0001g0017a0001c0002t0001g0062a0001c0002t0001g0074others(3): Show | 7 | HG00733.hp2 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4908T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501003 | ||||||
chr13:49501006
|
T | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(23): Show | 30 | HG01109.hp1 HG01257.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+4911T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501006 | ||||||
chr13:49501007
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.94+4912T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501007 | ||||||
chr13:49501010
|
TTTTTTGG | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(14): Show | 20 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+4921_94+4927del others(7): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501010 | |||||
chr13:49501011
|
T | G | 1 | a0001c0001t0002g0016 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.94+4916T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501011 | ||||||
chr13:49501011
|
TTTTTGG | T | 31 | a0001c0001t0002g0272a0001c0001t0003g0004a0001c0001t0003g0036others(28): Show | 37 | HG00558.hp2 HG00642.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+4921_94+4926del others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501011 | |||||
chr13:49501012
|
T | G | 2 | a0001c0002t0001g0078a0001c0002t0001g0079 | 2 | HG02148.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.94+4917T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501012 | ||||||
chr13:49501012
|
TTTTGG | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(29): Show | 36 | HG00408.hp2 HG01109.hp1 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.94+4921_94+4925del others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501012 | |||||
chr13:49501013
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+4918T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501013 | ||||||
chr13:49501015
|
TG | T | 12 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0001g0228others(9): Show | 14 | HG01106.hp1 HG01891.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+4922delG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501015 | |||||
chr13:49501016
|
G | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(176): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.94+4921G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501016 | ||||||
chr13:49501017
|
G | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(244): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.94+4922G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501017 | ||||||
chr13:49501021
|
T | G | 1 | a0001c0002t0001g0081 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.94+4926T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501021 | ||||||
chr13:49501052
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.94+4957C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501052 | ||||||
chr13:49501058
|
G | C | 2 | a0003c0006t0001g0069a0003c0006t0001g0070 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.94+4963G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501058 | ||||||
chr13:49501076
|
C | T | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0141 | 3 | HG02257.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+4981C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501076 | ||||||
chr13:49501087
|
C | G | 5 | a0001c0002t0001g0012a0001c0002t0001g0063a0001c0002t0001g0331others(2): Show | 7 | HG00280.hp1 HG01069.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4992C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501087 | ||||||
chr13:49501090
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0120others(12): Show | 17 | HG00621.hp1 HG02165.hp1 HG03490.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+4995C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501090 | ||||||
chr13:49501240
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+5145C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501240 | ||||||
chr13:49501245
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.94+5150T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501245 | ||||||
chr13:49501304
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(6): Show | 11 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+5209C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501304 | ||||||
chr13:49501382
|
A | G | 1 | a0001c0001t0003g0283 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.95-5253A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501382 | ||||||
chr13:49501730
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-4905G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501730 | ||||||
chr13:49501793
|
T | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.95-4842T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501793 | ||||||
chr13:49501938
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 17 | HG01257.hp2 HG02015.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-4697G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501938 | ||||||
chr13:49501943
|
G | A | 99 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0226others(96): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.95-4692G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501943 | ||||||
chr13:49501981
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-4654G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501981 | ||||||
chr13:49502037
|
T | C | 4 | a0001c0001t0002g0011a0001c0001t0002g0291a0001c0001t0002g0292others(1): Show | 6 | NA18953.hp2 NA18971.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4598T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502037 | ||||||
chr13:49502049
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.95-4586C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502049 | ||||||
chr13:49502071
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(24): Show | 32 | HG01109.hp1 HG01257.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.95-4564G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502071 | ||||||
chr13:49502093
|
A | T | 2 | a0003c0006t0001g0069a0003c0006t0001g0070 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.95-4542A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502093 | ||||||
chr13:49502213
|
A | T | 1 | a0001c0001t0002g0197 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.95-4422A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502213 | ||||||
chr13:49502312
|
AATTG | A | 9 | a0001c0001t0001g0136a0001c0001t0002g0022a0001c0001t0002g0023others(6): Show | 11 | HG01106.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-4319_95-4316del others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49502312 | |||||
chr13:49502622
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-4013C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502622 | ||||||
chr13:49502645
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.95-3990T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502645 | ||||||
chr13:49502745
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0042others(48): Show | 64 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.95-3890G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502745 | ||||||
chr13:49502779
|
G | A | 12 | a0001c0001t0001g0136a0001c0001t0001g0227a0001c0001t0001g0228others(9): Show | 14 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-3856G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502779 | ||||||
chr13:49503019
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.95-3616G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503019 | ||||||
chr13:49503166
|
C | T | 1 | a0001c0002t0001g0100 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.95-3469C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503166 | ||||||
chr13:49503310
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0199a0001c0001t0001g0233others(38): Show | 53 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.95-3325C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503310 | ||||||
chr13:49503451
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-3184C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503451 | ||||||
chr13:49503484
|
C | A | 1 | a0001c0001t0003g0311 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.95-3151C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503484 | ||||||
chr13:49503484
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.95-3151C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503484 | ||||||
chr13:49503499
|
T | C | 1 | a0001c0001t0003g0278 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.95-3136T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503499 | ||||||
chr13:49503542
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.95-3093G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503542 | ||||||
chr13:49503705
|
C | A | 1 | a0001c0001t0002g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-2930C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503705 | ||||||
chr13:49503752
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.95-2883A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503752 | ||||||
chr13:49503762
|
T | G | 55 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(52): Show | 64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-2873T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503762 | ||||||
chr13:49503961
|
T | G | 1 | a0001c0002t0001g0082 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.95-2674T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503961 | ||||||
chr13:49504003
|
C | A | 1 | a0001c0001t0002g0293 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.95-2632C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504003 | ||||||
chr13:49504133
|
A | C | 1 | a0001c0001t0002g0302 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.95-2502A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504133 | ||||||
chr13:49504167
|
A | T | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-2468A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504167 | ||||||
chr13:49504382
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.95-2253G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504382 | ||||||
chr13:49504481
|
CGCCCGGC others(71): Show |
C | 99 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0226others(96): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.95-2126_95-2049del others(78): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504481 | |||||
chr13:49504486
|
G | A | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0140others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2149G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504486 | ||||||
chr13:49504493
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0242 | 3 | HG01884.hp2 HG01891.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.95-2142C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504493 | ||||||
chr13:49504503
|
G | A | 55 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(52): Show | 64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-2132G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504503 | ||||||
chr13:49504513
|
GGGCGCCT others(119): Show |
G | 8 | a0001c0001t0001g0103a0001c0001t0001g0136a0001c0001t0002g0022others(5): Show | 9 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-2109_95-1984del | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504513 | |||||
chr13:49504516
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.95-2119C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504516 | ||||||
chr13:49504526
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(147): Show | 178 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.95-2109T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504526 | ||||||
chr13:49504526
|
T | TGGCCGCC others(245): Show |
1 | a0001c0001t0001g0129 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-2026_95-2025ins others(252): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504526 | |||||
chr13:49504530
|
C | T | 1 | a0001c0001t0002g0016 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.95-2105C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504530 | ||||||
chr13:49504591
|
T | TGGGGGGT others(42): Show |
105 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0024others(102): Show | 127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.95-2001_95-2000ins others(49): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504591 | |||||
chr13:49504610
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(17): Show | 22 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-2025C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504610 | ||||||
chr13:49504627
|
C | CCGGGAGG others(42): Show |
2 | a0001c0001t0001g0301a0001c0001t0001g0325 | 2 | HG01192.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.95-2001_95-2000ins others(49): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504627 | |||||
chr13:49504639
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-1996A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504639 | ||||||
chr13:49504666
|
A | G | 107 | a0001c0001t0001g0103a0001c0001t0001g0136a0001c0001t0001g0159others(104): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.95-1969A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504666 | ||||||
chr13:49504715
|
A | G | 44 | a0001c0001t0002g0272a0001c0001t0002g0280a0001c0001t0003g0004others(41): Show | 50 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.95-1920A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504715 | ||||||
chr13:49504732
|
G | A | 3 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336 | 3 | HG01517.hp2 HG01981.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.95-1903G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504732 | ||||||
chr13:49504752
|
C | G | 1 | a0001c0001t0002g0223 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.95-1883C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504752 | ||||||
chr13:49504761
|
G | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1874G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504761 | ||||||
chr13:49504774
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.95-1861G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504774 | ||||||
chr13:49504835
|
T | TA | 9 | a0001c0001t0001g0136a0001c0001t0002g0022a0001c0001t0002g0023others(6): Show | 11 | HG01106.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-1799dupA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504835 | |||||
chr13:49504865
|
T | C | 2 | a0001c0001t0001g0288a0001c0001t0001g0294 | 2 | HG02074.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.95-1770T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504865 | ||||||
chr13:49504920
|
A | G | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0140others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1715A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504920 | ||||||
chr13:49505113
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.95-1522A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505113 | ||||||
chr13:49505146
|
G | GA | 8 | a0001c0001t0003g0255a0001c0001t0003g0279a0001c0002t0001g0018others(5): Show | 9 | NA18942.hp2 NA18943.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1475dupA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49505146 | |||||
chr13:49505146
|
GA | G | 26 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(23): Show | 28 | HG01106.hp1 HG01109.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-1475delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49505146 | |||||
chr13:49505218
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-1417G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505218 | ||||||
chr13:49505245
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.95-1390C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505245 | ||||||
chr13:49505353
|
A | G | 4 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(1): Show | 4 | HG00735.hp2 HG03239.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1282A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505353 | ||||||
chr13:49505471
|
C | A | 1 | a0001c0001t0002g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.95-1164C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505471 | ||||||
chr13:49505625
|
G | A | 40 | a0001c0001t0001g0120a0001c0001t0002g0272a0001c0001t0002g0280others(37): Show | 46 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.95-1010G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505625 | ||||||
chr13:49505787
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.95-848C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505787 | ||||||
chr13:49505926
|
G | A | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0140others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-709G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505926 | ||||||
chr13:49505988
|
C | A | 1 | a0001c0001t0003g0257 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-647C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505988 | ||||||
chr13:49506223
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.95-412C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506223 | ||||||
chr13:49506233
|
T | TA | 17 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0049others(14): Show | 18 | HG00733.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-383dupA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49506233 | |||||
chr13:49506233
|
TA | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0235a0001c0001t0001g0244others(4): Show | 7 | HG01099.hp1 HG02897.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-383delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49506233 | |||||
chr13:49506325
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-310G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506325 | ||||||
chr13:49506456
|
A | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(18): Show | 23 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.95-179A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506456 | ||||||
chr13:49506501
|
A | C | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95-134A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506501 | ||||||
chr13:49506861
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.216+105A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49506861 | ||||||
chr13:49506898
|
C | CT | 235 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(232): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.216+165dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49506898 | |||||
chr13:49506898
|
C | CTT | 23 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0104others(20): Show | 23 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.216+164_216+165dup others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49506898 | |||||
chr13:49506898
|
CT | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+165delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49506898 | |||||
chr13:49506924
|
G | A | 11 | a0001c0001t0001g0136a0001c0001t0001g0227a0001c0001t0001g0242others(8): Show | 13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+168G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49506924 | ||||||
chr13:49506997
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0190 | 2 | HG01192.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.216+241G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49506997 | ||||||
chr13:49507004
|
C | T | 2 | a0003c0006t0001g0069a0003c0006t0001g0070 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.216+248C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507004 | ||||||
chr13:49507032
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.216+276T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507032 | ||||||
chr13:49507048
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.216+292T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507048 | ||||||
chr13:49507070
|
A | AT | 6 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+322dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49507070 | |||||
chr13:49507138
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.216+382C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507138 | ||||||
chr13:49507187
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+431G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507187 | ||||||
chr13:49507222
|
C | T | 100 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(97): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.216+466C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507222 | ||||||
chr13:49507382
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.216+626A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507382 | ||||||
chr13:49507744
|
T | G | 1 | a0001c0001t0002g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.216+988T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507744 | ||||||
chr13:49507960
|
C | T | 1 | a0001c0005t0002g0178 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.216+1204C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507960 | ||||||
chr13:49508120
|
A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(259): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.216+1364A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508120 | ||||||
chr13:49508153
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.216+1397A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508153 | ||||||
chr13:49508160
|
A | ATATGTAT others(19): Show |
15 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 17 | HG01070.hp1 HG01257.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.216+1428_216+1453d others(28): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508160 | |||||
chr13:49508160
|
A | ATATGTAT others(45): Show |
1 | a0001c0001t0001g0052 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.216+1453_216+1454i others(54): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508160 | |||||
chr13:49508186
|
G | GTATGTAT others(19): Show |
51 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0042others(48): Show | 64 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.216+1450_216+1475d others(28): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508186 | |||||
chr13:49508258
|
G | A | 1 | a0001c0002t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.216+1502G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508258 | ||||||
chr13:49508297
|
A | G | 11 | a0001c0001t0001g0136a0001c0001t0001g0227a0001c0001t0001g0242others(8): Show | 13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+1541A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508297 | ||||||
chr13:49508319
|
AATATATT others(9): Show |
A | 66 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(63): Show | 75 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.216+1587_216+1602d others(18): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508319 | |||||
chr13:49508332
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1576A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508332 | ||||||
chr13:49508336
|
A | C | 60 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.216+1580A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508336 | ||||||
chr13:49508343
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0242 | 2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.216+1587A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508343 | ||||||
chr13:49508344
|
C | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0242 | 2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.216+1588C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508344 | ||||||
chr13:49508352
|
A | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.216+1596A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508352 | ||||||
chr13:49508536
|
T | G | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0140others(1): Show | 4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1780T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508536 | ||||||
chr13:49508612
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.216+1856T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508612 | ||||||
chr13:49508846
|
C | T | 1 | a0001c0005t0002g0178 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.216+2090C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508846 | ||||||
chr13:49508965
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.216+2209A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508965 | ||||||
chr13:49509214
|
A | AT | 114 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(111): Show | 135 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.216+2473dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49509214 | |||||
chr13:49509214
|
AT | A | 24 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(21): Show | 27 | HG01074.hp2 HG01081.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.216+2473delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49509214 | |||||
chr13:49509276
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0228 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.216+2520G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509276 | ||||||
chr13:49509376
|
C | T | 55 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(52): Show | 64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.216+2620C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509376 | ||||||
chr13:49509446
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0242 | 2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.216+2690C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509446 | ||||||
chr13:49509462
|
C | T | 55 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(52): Show | 64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.216+2706C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509462 | ||||||
chr13:49509520
|
T | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(13): Show | 19 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.216+2764T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509520 | ||||||
chr13:49509562
|
C | G | 1 | a0001c0002t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.216+2806C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509562 | ||||||
chr13:49509745
|
A | G | 1 | a0001c0001t0003g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.216+2989A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509745 | ||||||
chr13:49509831
|
T | G | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+3075T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509831 | ||||||
chr13:49510012
|
C | CGT | 12 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0113others(9): Show | 13 | HG01074.hp1 HG01243.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.217-3029_217-3028d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49510012 | |||||
chr13:49510135
|
C | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-2924C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510135 | ||||||
chr13:49510201
|
C | T | 16 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 18 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217-2858C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510201 | ||||||
chr13:49510207
|
G | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0176 | 3 | HG00099.hp2 HG01346.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.217-2852G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510207 | ||||||
chr13:49510286
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0042others(52): Show | 68 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.217-2773A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510286 | ||||||
chr13:49510344
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.217-2715A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510344 | ||||||
chr13:49510700
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.217-2359G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510700 | ||||||
chr13:49511073
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | NA18947.hp1 NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.217-1986T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511073 | ||||||
chr13:49511127
|
A | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0199a0001c0001t0001g0233others(39): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.217-1932A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511127 | ||||||
chr13:49511327
|
C | CTT | 209 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 266 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.217-1717_217-1716d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49511327 | |||||
chr13:49511327
|
C | CTTT | 47 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0104others(44): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.217-1718_217-1716d others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49511327 | |||||
chr13:49511327
|
CT | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0043others(15): Show | 20 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.217-1716delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49511327 | |||||
chr13:49511349
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.217-1710G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511349 | ||||||
chr13:49511357
|
G | A | 1 | a0001c0002t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.217-1702G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511357 | ||||||
chr13:49511387
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0199others(43): Show | 59 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.217-1672C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511387 | ||||||
chr13:49511404
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0195 | 2 | HG01123.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.217-1655G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511404 | ||||||
chr13:49511413
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(11): Show | 16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.217-1646G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511413 | ||||||
chr13:49511682
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.217-1377G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511682 | ||||||
chr13:49511734
|
C | A | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.217-1325C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511734 | ||||||
chr13:49511742
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0228 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.217-1317A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511742 | ||||||
chr13:49512108
|
A | G | 102 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0008others(99): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.217-951A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512108 | ||||||
chr13:49512117
|
T | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(32): Show | 41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-942T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512117 | ||||||
chr13:49512130
|
G | T | 103 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(100): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.217-929G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512130 | ||||||
chr13:49512190
|
T | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.217-869T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512190 | ||||||
chr13:49512293
|
T | G | 1 | a0001c0001t0002g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217-766T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512293 | ||||||
chr13:49512314
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(32): Show | 41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-745C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512314 | ||||||
chr13:49512354
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.217-705T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512354 | ||||||
chr13:49512734
|
C | G | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-325C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512734 | ||||||
chr13:49512973
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0228 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.217-86G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512973 | ||||||
chr13:49513006
|
T | C | 72 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0008others(69): Show | 98 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.217-53T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49513006 | ||||||
chr13:49513328
|
A | AT | 50 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 58 | HG01070.hp1 HG01074.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.324+181dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49513328 | |||||
chr13:49513328
|
AT | A | 115 | a0001c0001t0001g0114a0001c0001t0001g0136a0001c0001t0001g0163others(112): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.324+181delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49513328 | |||||
chr13:49513328
|
ATT | A | 11 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(8): Show | 11 | HG00673.hp1 HG01109.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+180_324+181del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49513328 | |||||
chr13:49513351
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+185A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513351 | ||||||
chr13:49513392
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.324+226A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513392 | ||||||
chr13:49513403
|
TCACTGCA others(20): Show |
T | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+238_324+264del others(27): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513403 | ||||||
chr13:49513446
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+280T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513446 | ||||||
chr13:49513449
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.324+283G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513449 | ||||||
chr13:49513450
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+284C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513450 | ||||||
chr13:49513451
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+285C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513451 | ||||||
chr13:49513452
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+286T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513452 | ||||||
chr13:49513454
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+288C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513454 | ||||||
chr13:49513456
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.324+290G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513456 | ||||||
chr13:49513530
|
C | T | 11 | a0001c0001t0001g0136a0001c0001t0001g0227a0001c0001t0001g0242others(8): Show | 13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+364C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513530 | ||||||
chr13:49513539
|
C | T | 20 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0039others(17): Show | 26 | HG00408.hp1 HG01952.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.324+373C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513539 | ||||||
chr13:49513613
|
G | T | 1 | a0001c0001t0002g0170 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.324+447G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513613 | ||||||
chr13:49513640
|
TA | T | 103 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(100): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.324+475delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513640 | ||||||
chr13:49513874
|
C | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(16): Show | 21 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.324+708C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513874 | ||||||
chr13:49513877
|
T | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(16): Show | 21 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.324+711T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513877 | ||||||
chr13:49513896
|
G | A | 2 | a0003c0006t0001g0069a0003c0006t0001g0070 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.324+730G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513896 | ||||||
chr13:49513927
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.324+761G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513927 | ||||||
chr13:49513997
|
G | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(32): Show | 41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.324+831G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513997 | ||||||
chr13:49514020
|
A | G | 1 | a0001c0001t0002g0232 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.324+854A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514020 | ||||||
chr13:49514221
|
A | G | 337 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(334): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.324+1055A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514221 | ||||||
chr13:49514314
|
G | C | 1 | a0001c0001t0003g0261 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.324+1148G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514314 | ||||||
chr13:49514709
|
G | C | 1 | a0001c0002t0001g0329 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.324+1543G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514709 | ||||||
chr13:49514762
|
TA | T | 221 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(218): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.324+1611delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49514762 | |||||
chr13:49514939
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+1773A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514939 | ||||||
chr13:49515109
|
G | A | 4 | a0001c0002t0001g0019a0001c0002t0001g0088a0001c0002t0001g0089others(1): Show | 5 | HG00609.hp2 HG02083.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1943G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515109 | ||||||
chr13:49515138
|
G | A | 15 | a0001c0002t0001g0012a0001c0002t0001g0040a0001c0002t0001g0063others(12): Show | 18 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1972G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515138 | ||||||
chr13:49515335
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(32): Show | 41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.324+2169C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515335 | ||||||
chr13:49515455
|
T | TAC | 23 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0123others(20): Show | 31 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.324+2337_324+2338d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
T | TACAC | 7 | a0001c0001t0001g0128a0001c0001t0002g0204a0001c0002t0001g0075others(4): Show | 7 | HG00735.hp1 HG01106.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+2335_324+2338d others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
T | TACACACA others(1): Show |
3 | a0001c0002t0001g0091a0001c0002t0001g0094a0001c0002t0001g0108 | 3 | HG01070.hp2 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.324+2331_324+2338d others(10): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TAC | T | 11 | a0001c0001t0001g0103a0001c0001t0002g0026a0001c0001t0002g0132others(8): Show | 12 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+2337_324+2338d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACAC | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(36): Show | 45 | HG00408.hp2 HG00741.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.324+2335_324+2338d others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACAC | T | 46 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0072others(43): Show | 56 | HG00558.hp2 HG00639.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.324+2333_324+2338d others(8): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(1): Show |
T | 20 | a0001c0001t0001g0227a0001c0001t0001g0245a0001c0001t0001g0246others(17): Show | 22 | HG00280.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.324+2331_324+2338d others(10): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0243a0001c0001t0002g0023a0001c0001t0002g0139others(2): Show | 6 | HG01106.hp1 HG01123.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+2329_324+2338d others(12): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(7): Show |
T | 7 | a0001c0001t0001g0136a0001c0001t0002g0022a0001c0001t0002g0133others(4): Show | 8 | HG02486.hp1 HG03098.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2325_324+2338d others(16): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(9): Show |
T | 49 | a0001c0001t0001g0002a0001c0001t0001g0199a0001c0001t0001g0233others(46): Show | 62 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.324+2323_324+2338d others(18): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(11): Show |
T | 63 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0008others(60): Show | 88 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.324+2321_324+2338d others(20): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0002g0194 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.324+2317_324+2338d others(24): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(17): Show |
T | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(31): Show | 40 | HG01070.hp1 HG01109.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.324+2315_324+2338d others(26): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515455
|
TACACACA others(21): Show |
T | 2 | a0001c0001t0001g0054a0001c0001t0002g0169 | 2 | HG01257.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.324+2311_324+2338d others(30): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | |||||
chr13:49515489
|
CACACACA others(8): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.324+2324_324+2338d others(17): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515489 | ||||||
chr13:49515507
|
C | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0325 | 2 | HG01192.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.324+2341C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515507 | ||||||
chr13:49515547
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(11): Show | 16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.324+2381C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515547 | ||||||
chr13:49515708
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 104 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.325-2310C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515708 | ||||||
chr13:49515733
|
G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0291a0001c0001t0002g0292others(1): Show | 6 | NA18953.hp2 NA18971.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-2285G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515733 | ||||||
chr13:49515889
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.325-2129C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515889 | ||||||
chr13:49516069
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.325-1949G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516069 | ||||||
chr13:49516176
|
A | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0042others(50): Show | 63 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.325-1842A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516176 | ||||||
chr13:49516321
|
C | G | 1 | a0001c0001t0002g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-1697C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516321 | ||||||
chr13:49516335
|
A | G | 1 | a0001c0002t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.325-1683A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516335 | ||||||
chr13:49516338
|
C | G | 1 | a0001c0001t0002g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-1680C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516338 | ||||||
chr13:49516494
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0113others(21): Show | 30 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.325-1524T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516494 | ||||||
chr13:49516586
|
T | G | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.325-1432T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516586 | ||||||
chr13:49516708
|
C | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.325-1310C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516708 | ||||||
chr13:49516745
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-1273C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516745 | ||||||
chr13:49516965
|
C | T | 1 | a0001c0001t0002g0293 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.325-1053C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516965 | ||||||
chr13:49516972
|
C | T | 15 | a0001c0002t0001g0012a0001c0002t0001g0040a0001c0002t0001g0063others(12): Show | 18 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-1046C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516972 | ||||||
chr13:49516974
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.325-1044A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516974 | ||||||
chr13:49517013
|
T | C | 1 | a0001c0002t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.325-1005T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517013 | ||||||
chr13:49517022
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG01109.hp1 HG02451.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-996C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517022 | ||||||
chr13:49517598
|
G | GAGA | 13 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 16 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.325-418_325-416dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49517598 | |||||
chr13:49517736
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.325-282G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517736 | ||||||
chr13:49517956
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.325-62C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517956 | ||||||
chr13:49517991
|
TACTC | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(224): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.325-25_325-22delCT others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49517991 | |||||
chr13:49518193
|
G | A | 1 | a0003c0006t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458+42G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518193 | ||||||
chr13:49518324
|
CTA | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.458+189_458+190del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518324 | |||||
chr13:49518330
|
A | C | 1 | a0001c0001t0003g0279 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.458+179A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518330 | ||||||
chr13:49518330
|
A | T | 1 | a0001c0002t0001g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.458+179A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518330 | ||||||
chr13:49518331
|
T | A | 1 | a0001c0002t0001g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.458+180T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518331 | ||||||
chr13:49518350
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(224): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.458+199T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518350 | ||||||
chr13:49518429
|
C | T | 2 | a0003c0006t0001g0069a0003c0006t0001g0070 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.458+278C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518429 | ||||||
chr13:49518460
|
G | T | 15 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(12): Show | 17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.458+309G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518460 | ||||||
chr13:49518597
|
T | TTAATCCT others(22): Show |
1 | a0001c0002t0001g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.458+449_458+477dup others(29): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518597 | |||||
chr13:49518705
|
G | A | 15 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(12): Show | 17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.458+554G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518705 | ||||||
chr13:49518711
|
G | A | 125 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(122): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.458+560G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518711 | ||||||
chr13:49518717
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(6): Show | 11 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.458+566G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518717 | ||||||
chr13:49518834
|
A | AT | 55 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(52): Show | 64 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.458+702dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | |||||
chr13:49518834
|
A | ATT | 6 | a0001c0001t0001g0125a0002c0003t0001g0015a0002c0003t0001g0041others(3): Show | 7 | HG00621.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+701_458+702dup others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | |||||
chr13:49518834
|
A | ATTT | 9 | a0001c0001t0001g0136a0001c0001t0001g0227a0001c0001t0002g0022others(6): Show | 11 | HG01106.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.458+700_458+702dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | |||||
chr13:49518834
|
A | ATTTT | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.458+699_458+702dup others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | |||||
chr13:49518834
|
AT | A | 116 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0005others(113): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.458+702delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | |||||
chr13:49518839
|
T | A | 1 | a0001c0001t0002g0173 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.458+688T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518839 | ||||||
chr13:49518859
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+708A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518859 | ||||||
chr13:49518898
|
C | G | 71 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0008others(68): Show | 96 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.458+747C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518898 | ||||||
chr13:49518899
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.458+748G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518899 | ||||||
chr13:49518960
|
C | T | 110 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0005others(107): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.458+809C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518960 | ||||||
chr13:49518961
|
G | A | 11 | a0001c0001t0002g0011a0001c0001t0002g0039a0001c0001t0002g0200others(8): Show | 14 | NA18612.hp1 NA18946.hp1 NA18953.hp2 others(11): Show |
intron_variant | MODIFIER | c.458+810G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518961 | ||||||
chr13:49518981
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+830G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518981 | ||||||
chr13:49518982
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+831C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518982 | ||||||
chr13:49518983
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+832C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518983 | ||||||
chr13:49518983
|
C | T | 13 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 16 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.458+832C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518983 | ||||||
chr13:49518984
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+833C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518984 | ||||||
chr13:49518987
|
T | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 53 | HG00733.hp1 HG01070.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.458+836T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518987 | ||||||
chr13:49518990
|
C | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0228a0001c0001t0002g0154others(1): Show | 4 | HG00733.hp1 HG01891.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+839C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518990 | ||||||
chr13:49518992
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+841C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518992 | ||||||
chr13:49518993
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(25): Show | 32 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.458+842G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518993 | ||||||
chr13:49519051
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458+900G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519051 | ||||||
chr13:49519057
|
A | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0275 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.458+906A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519057 | ||||||
chr13:49519062
|
C | G | 11 | a0001c0001t0001g0136a0001c0001t0001g0227a0001c0001t0001g0242others(8): Show | 13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.458+911C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519062 | ||||||
chr13:49519078
|
G | A | 2 | a0001c0001t0002g0164a0001c0002t0002g0077 | 2 | HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.458+927G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519078 | ||||||
chr13:49519109
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.458+958A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519109 | ||||||
chr13:49519169
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+1018G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519169 | ||||||
chr13:49519169
|
G | C | 1 | a0001c0001t0002g0194 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.458+1018G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519169 | ||||||
chr13:49519191
|
G | A | 7 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 10 | HG01975.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.458+1040G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519191 | ||||||
chr13:49519307
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.458+1156A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519307 | ||||||
chr13:49519316
|
G | A | 125 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(122): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.458+1165G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519316 | ||||||
chr13:49519692
|
C | CTTGAG | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.459-1201_459-1197d others(7): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49519692 | |||||
chr13:49519721
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(11): Show | 16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-1173T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519721 | ||||||
chr13:49519757
|
T | C | 2 | a0001c0001t0001g0288a0001c0001t0001g0294 | 2 | HG02074.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.459-1137T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519757 | ||||||
chr13:49519848
|
G | A | 15 | a0001c0002t0001g0012a0001c0002t0001g0040a0001c0002t0001g0063others(12): Show | 18 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.459-1046G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519848 | ||||||
chr13:49519868
|
A | G | 43 | a0001c0001t0002g0280a0001c0001t0003g0004a0001c0001t0003g0036others(40): Show | 49 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.459-1026A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519868 | ||||||
chr13:49519869
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.459-1025T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519869 | ||||||
chr13:49519886
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0002g0022a0001c0001t0002g0023others(6): Show | 11 | HG01106.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-1008G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519886 | ||||||
chr13:49519954
|
T | C | 42 | a0001c0001t0002g0280a0001c0001t0003g0004a0001c0001t0003g0036others(39): Show | 48 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.459-940T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519954 | ||||||
chr13:49520037
|
A | G | 2 | a0003c0006t0001g0069a0003c0006t0001g0070 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.459-857A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520037 | ||||||
chr13:49520046
|
C | CT | 14 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(11): Show | 16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-844dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49520046 | |||||
chr13:49520051
|
G | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(239): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.459-843G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520051 | ||||||
chr13:49520087
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.459-807G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520087 | ||||||
chr13:49520112
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-782A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520112 | ||||||
chr13:49520140
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-754C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520140 | ||||||
chr13:49520152
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-742G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520152 | ||||||
chr13:49520182
|
G | A | 2 | a0001c0001t0002g0165a0001c0001t0002g0193 | 2 | NA18969.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.459-712G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520182 | ||||||
chr13:49520185
|
T | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.459-709T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520185 | ||||||
chr13:49520236
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.459-658G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520236 | ||||||
chr13:49520299
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-595G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520299 | ||||||
chr13:49520367
|
A | T | 1 | a0001c0001t0002g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.459-527A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520367 | ||||||
chr13:49520474
|
T | G | 45 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0032others(42): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.459-420T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520474 | ||||||
chr13:49520482
|
A | C | 1 | a0001c0001t0003g0261 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.459-412A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520482 | ||||||
chr13:49520557
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.459-337A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520557 | ||||||
chr13:49520573
|
A | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(12): Show | 17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.459-321A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520573 | ||||||
chr13:49520988
|
T | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(12): Show | 17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.505+48T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49520988 | ||||||
chr13:49520991
|
A | G | 124 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0005others(121): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.505+51A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49520991 | ||||||
chr13:49521026
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+86G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521026 | ||||||
chr13:49521078
|
G | T | 1 | a0001c0001t0002g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.505+138G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521078 | ||||||
chr13:49521307
|
A | G | 125 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(122): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.505+367A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521307 | ||||||
chr13:49521546
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(1): Show | 4 | HG00735.hp2 HG03239.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-497G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521546 | ||||||
chr13:49521685
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(26): Show | 33 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.506-358G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521685 | ||||||
chr13:49521817
|
C | G | 174 | a0001c0001t0001g0163a0001c0001t0001g0226a0001c0001t0002g0001others(171): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.506-226C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521817 | ||||||
chr13:49521822
|
T | A | 1 | a0001c0001t0002g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.506-221T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521822 | ||||||
chr13:49521974
|
T | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 11 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-69T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521974 | ||||||
chr13:49521991
|
C | G | 72 | a0001c0001t0001g0163a0001c0001t0002g0001a0001c0001t0002g0008others(69): Show | 98 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.506-52C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521991 | ||||||
chr13:49522148
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.570+41C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522148 | ||||||
chr13:49522174
|
A | G | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0141 | 3 | HG02257.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570+67A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522174 | ||||||
chr13:49522306
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+199A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522306 | ||||||
chr13:49522531
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0225 | 3 | NA19004.hp2 NA19011.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.570+424C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522531 | ||||||
chr13:49522564
|
G | GATT | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.570+460_570+462dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 49522564 | |||||
chr13:49522581
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.570+474A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522581 | ||||||
chr13:49522714
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-461A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522714 | ||||||
chr13:49522755
|
TG | T | 41 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(38): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.571-416delG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 49522755 | |||||
chr13:49522758
|
GGT | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0119a0001c0001t0001g0124others(16): Show | 26 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-416_571-415del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | ||||||
chr13:49522758
|
GGTT | G | 36 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0120others(33): Show | 38 | HG00544.hp1 HG00621.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.571-416_571-414del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | ||||||
chr13:49522758
|
GGTTT | G | 103 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0113others(100): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.571-416_571-413del others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | ||||||
chr13:49522758
|
GGTTTT | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0002g0166others(2): Show | 5 | HG01496.hp2 HG02970.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-416_571-412del others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | ||||||
chr13:49522759
|
G | T | 21 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0249others(18): Show | 21 | HG00408.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-416G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522759 | ||||||
chr13:49522763
|
T | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.571-412T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522763 | ||||||
chr13:49522765
|
TTG | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0046others(20): Show | 27 | HG01070.hp1 HG01257.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.571-408_571-407del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 49522765 | |||||
chr13:49522766
|
TG | T | 15 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0056others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-408delG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522766 | ||||||
chr13:49522767
|
G | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(230): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.571-408G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522767 | ||||||
chr13:49522771
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.571-404T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522771 | ||||||
chr13:49522807
|
C | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-368C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522807 | ||||||
chr13:49523487
|
A | G | 8 | a0001c0001t0002g0210a0001c0001t0002g0218a0001c0001t0002g0219others(5): Show | 8 | HG02074.hp1 NA18946.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+246A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523487 | ||||||
chr13:49523491
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.637+250A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523491 | ||||||
chr13:49523576
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.637+335T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523576 | ||||||
chr13:49523623
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0103 | 3 | HG02280.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+382G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523623 | ||||||
chr13:49523626
|
CTGT | C | 3 | a0001c0001t0002g0009a0001c0001t0002g0169a0001c0001t0002g0230 | 5 | HG00438.hp2 HG00544.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+387_637+389del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 49523626 | |||||
chr13:49523754
|
C | T | 42 | a0001c0001t0003g0004a0001c0001t0003g0036a0001c0001t0003g0037others(39): Show | 48 | HG00558.hp2 HG00642.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.638-331C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523754 | ||||||
chr13:49523843
|
T | C | 138 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(135): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.638-242T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523843 | ||||||
chr13:49523870
|
T | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0099 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.638-215T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523870 | ||||||
chr13:49523919
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-166A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523919 | ||||||
chr13:49523930
|
T | A | 1 | a0001c0001t0002g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.638-155T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523930 | ||||||
chr13:49524240
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.769+24G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524240 | ||||||
chr13:49524240
|
G | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(86): Show | 103 | HG00558.hp2 HG00642.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.769+24G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524240 | ||||||
chr13:49524271
|
TAAAAC | T | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.769+64_769+68delAC others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49524271 | |||||
chr13:49524305
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.769+89C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524305 | ||||||
chr13:49524477
|
C | CT | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(10): Show | 15 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.769+275dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49524477 | |||||
chr13:49524477
|
CT | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0043others(35): Show | 45 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.769+275delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49524477 | |||||
chr13:49524497
|
G | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0104others(17): Show | 23 | HG00621.hp1 HG01074.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.769+281G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524497 | ||||||
chr13:49524567
|
C | T | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.769+351C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524567 | ||||||
chr13:49524568
|
A | G | 132 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(129): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.769+352A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524568 | ||||||
chr13:49524727
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.769+511C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524727 | ||||||
chr13:49524755
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.769+539C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524755 | ||||||
chr13:49524766
|
A | G | 130 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(127): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.769+550A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524766 | ||||||
chr13:49524791
|
T | G | 3 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206 | 3 | HG00735.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.769+575T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524791 | ||||||
chr13:49524830
|
T | C | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.769+614T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524830 | ||||||
chr13:49524870
|
C | G | 1 | a0001c0001t0003g0276 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.769+654C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524870 | ||||||
chr13:49524965
|
G | A | 1 | a0001c0002t0001g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.769+749G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524965 | ||||||
chr13:49525021
|
A | C | 16 | a0001c0002t0001g0010a0001c0002t0001g0012a0001c0002t0001g0040others(13): Show | 21 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.769+805A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525021 | ||||||
chr13:49525052
|
C | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(218): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.769+836C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525052 | ||||||
chr13:49525192
|
G | A | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.769+976G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525192 | ||||||
chr13:49525303
|
A | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(87): Show | 105 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.770-1084A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525303 | ||||||
chr13:49525404
|
C | T | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.770-983C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525404 | ||||||
chr13:49525439
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.770-948A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525439 | ||||||
chr13:49525595
|
TTATAAA | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-787_770-782del others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49525595 | |||||
chr13:49525603
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-784A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525603 | ||||||
chr13:49525644
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.770-743G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525644 | ||||||
chr13:49525954
|
T | A | 126 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(123): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.770-433T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525954 | ||||||
chr13:49525960
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.770-427G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525960 | ||||||
chr13:49525979
|
GCC | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-407_770-406del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525979 | ||||||
chr13:49526168
|
CA | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 43 | HG01070.hp1 HG01070.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.770-197delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | |||||
chr13:49526168
|
CAA | C | 68 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0042others(65): Show | 78 | HG00558.hp2 HG00642.hp2 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.770-198_770-197del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | |||||
chr13:49526168
|
CAAA | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(39): Show | 51 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.770-199_770-197del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | |||||
chr13:49526168
|
CAAAA | C | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.770-200_770-197del others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | |||||
chr13:49526184
|
A | G | 133 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0242others(130): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.770-203A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526184 | ||||||
chr13:49526185
|
A | G | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0116others(2): Show | 5 | HG01109.hp2 HG01978.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-202A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526185 | ||||||
chr13:49526191
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.770-196G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526191 | ||||||
chr13:49526192
|
A | G | 1 | a0001c0002t0001g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.770-195A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526192 | ||||||
chr13:49526253
|
T | C | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.770-134T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526253 | ||||||
chr13:49526325
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-62T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526325 | ||||||
chr13:49526487
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0071others(9): Show | 14 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.841+29C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526487 | ||||||
chr13:49526491
|
GTT | G | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.841+36_841+37delTT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49526491 | |||||
chr13:49526501
|
ATATT | A | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.841+47_841+50delTT others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49526501 | |||||
chr13:49526511
|
C | T | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.841+53C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526511 | ||||||
chr13:49526531
|
G | A | 131 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(128): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.841+73G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526531 | ||||||
chr13:49526532
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(11): Show | 16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.841+74T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526532 | ||||||
chr13:49526620
|
T | C | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+162T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526620 | ||||||
chr13:49526621
|
G | C | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+163G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526621 | ||||||
chr13:49526646
|
C | T | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+188C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526646 | ||||||
chr13:49526702
|
G | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.841+244G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526702 | ||||||
chr13:49526762
|
A | G | 136 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(133): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.841+304A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526762 | ||||||
chr13:49526799
|
T | C | 3 | a0001c0001t0002g0210a0001c0001t0002g0213a0001c0001t0002g0224 | 3 | HG00438.hp1 NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.841+341T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526799 | ||||||
chr13:49526937
|
C | T | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+479C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526937 | ||||||
chr13:49526958
|
G | A | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+500G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526958 | ||||||
chr13:49527010
|
T | C | 1 | a0001c0002t0001g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.841+552T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527010 | ||||||
chr13:49527023
|
G | A | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+565G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527023 | ||||||
chr13:49527028
|
G | C | 8 | a0001c0002t0001g0018a0001c0002t0001g0021a0001c0002t0001g0083others(5): Show | 10 | HG02040.hp1 NA18943.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.841+570G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527028 | ||||||
chr13:49527033
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0119others(12): Show | 19 | HG00621.hp1 HG02165.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.841+575C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527033 | ||||||
chr13:49527054
|
GA | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(42): Show | 56 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.841+608delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49527054 | |||||
chr13:49527060
|
A | AAAC | 137 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(134): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.841+604_841+605ins others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49527060 | |||||
chr13:49527066
|
AC | A | 43 | a0001c0001t0003g0004a0001c0001t0003g0036a0001c0001t0003g0037others(40): Show | 49 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.841+609delC | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527066 | ||||||
chr13:49527067
|
C | A | 1 | a0001c0001t0002g0173 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.841+609C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527067 | ||||||
chr13:49527068
|
A | C | 1 | a0001c0001t0002g0173 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.841+610A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527068 | ||||||
chr13:49527080
|
AC | A | 141 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(138): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.841+623delC | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527080 | ||||||
chr13:49527390
|
C | T | 116 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(113): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.841+932C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527390 | ||||||
chr13:49527518
|
A | T | 140 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(137): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-993A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527518 | ||||||
chr13:49527527
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 6 | HG02818.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-984C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527527 | ||||||
chr13:49527927
|
T | G | 140 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(137): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-584T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527927 | ||||||
chr13:49527940
|
G | GTGTTT | 140 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(137): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-570_842-569ins others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49527940 | |||||
chr13:49527995
|
T | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0035others(13): Show | 19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.842-516T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527995 | ||||||
chr13:49528083
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0024others(224): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.842-428C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49528083 | ||||||
chr13:49528121
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.842-390G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49528121 | ||||||
chr13:49528236
|
T | A | 140 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(137): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-275T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49528236 |