geneid | 153918 |
---|---|
ensemblid | ENSG00000118491.10 |
hgncid | 21174 |
symbol | ZC2HC1B |
name | zinc finger C2HC-type containing 1B |
refseq_nuc | NM_001013623.3 |
refseq_prot | NP_001013645.1 |
ensembl_nuc | ENST00000237275.9 |
ensembl_prot | ENSP00000237275.6 |
mane_status | MANE Select |
chr | chr6 |
start | 143864474 |
end | 143938343 |
strand | + |
ver | v1.2 |
region | chr6:143864474-143938343 |
region5000 | chr6:143859474-143943343 |
regionname0 | ZC2HC1B_chr6_143864474_143938343 |
regionname5000 | ZC2HC1B_chr6_143859474_143943343 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 222 | 315 | 72 | 54 | 143 | 6 | 38 | 109 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0002 | 0/0 | 222 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0003 | 0/0 | 222 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0004 | 0/0 | 222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 669 | 315 | 72 | 54 | 143 | 6 | 38 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
c0002 | 0/0 | 669 | 11 | 11 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
c0003 | 0/0 | 669 | 3 | 3 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
c0004 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 283 | 330 | 86 | 54 | 144 | 6 | 38 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 669 | 315 | 72 | 54 | 143 | 6 | 38 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0002c0002 | 0/0 | 669 | 11 | 11 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0003c0003 | 0/0 | 669 | 3 | 3 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0004c0004 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 951 | 315 | 72 | 54 | 143 | 6 | 38 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0002c0002t0001 | 0/0 | 951 | 11 | 11 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0003c0003t0001 | 0/0 | 951 | 3 | 3 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
a0004c0004t0001 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | copy fasta | chr6 | 143859474 | 143943343 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18965 | hp2 | a0004 | c0004 | t0001 | g0057 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ASW | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02109 | hp1 | a0003 | c0003 | t0001 | g0033 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0206 | REF | REF | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0216 | REF | REF | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:143864555
|
C | T | 1 | a0002 | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
missense_variant | MODERATE | c.16C>T | p.Pro6Ser | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/8 | 82/951 | 16/669 | 6/222 | chr6 | 143864555 | ||
chr6:143886128
|
G | C | 1 | a0003 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.187G>C | p.Val63Leu | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/8 | 253/951 | 187/669 | 63/222 | chr6 | 143886128 | ||
chr6:143886132
|
A | C | 1 | a0004 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.191A>C | p.Lys64Thr | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/8 | 257/951 | 191/669 | 64/222 | chr6 | 143886132 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:143864781
|
T | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+214T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143864781 | ||||||
chr6:143864844
|
A | AG | 4 | a0001c0001t0001g0005a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 5 | HG00408.hp2 HG02071.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+278dupG | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143864844 | |||||
chr6:143864862
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+295A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143864862 | ||||||
chr6:143864910
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.28+343T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143864910 | ||||||
chr6:143865116
|
T | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+549T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865116 | ||||||
chr6:143865196
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.28+629T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865196 | ||||||
chr6:143865374
|
T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+807T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865374 | ||||||
chr6:143865385
|
C | A | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+818C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865385 | ||||||
chr6:143865385
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28+818C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865385 | ||||||
chr6:143865407
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.28+840A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865407 | ||||||
chr6:143865638
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+1071G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865638 | ||||||
chr6:143865640
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1073G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865640 | ||||||
chr6:143865720
|
T | TAGAA | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.28+1154_28+1157dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143865720 | |||||
chr6:143865812
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1245A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865812 | ||||||
chr6:143865853
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1286G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865853 | ||||||
chr6:143865859
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.28+1292G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865859 | ||||||
chr6:143865982
|
A | AT | 5 | a0001c0001t0001g0002a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 6 | HG03927.hp1 NA18952.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.28+1420dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143865982 | |||||
chr6:143866102
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1535G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866102 | ||||||
chr6:143866145
|
A | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(156): Show | 162 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.28+1578A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866145 | ||||||
chr6:143866176
|
C | T | 37 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0118others(34): Show | 37 | HG00140.hp2 HG00673.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+1609C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866176 | ||||||
chr6:143866255
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.28+1688C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866255 | ||||||
chr6:143866350
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.28+1783C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866350 | ||||||
chr6:143866384
|
A | G | 37 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0118others(34): Show | 37 | HG00140.hp2 HG00673.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+1817A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866384 | ||||||
chr6:143866393
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.28+1826C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866393 | ||||||
chr6:143866491
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(83): Show | 88 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.28+1924C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866491 | ||||||
chr6:143866588
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(10): Show | 13 | HG00733.hp1 HG01258.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+2021A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866588 | ||||||
chr6:143866815
|
ATATT | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0322 | 3 | HG02109.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28+2251_28+2254del others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143866815 | |||||
chr6:143867039
|
T | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+2472T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867039 | ||||||
chr6:143867091
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.28+2524T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867091 | ||||||
chr6:143867098
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+2531G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867098 | ||||||
chr6:143867355
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(10): Show | 13 | HG00733.hp1 HG01258.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+2788A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867355 | ||||||
chr6:143867410
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.28+2843C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867410 | ||||||
chr6:143867427
|
C | T | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+2860C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867427 | ||||||
chr6:143867580
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.28+3013C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867580 | ||||||
chr6:143867628
|
T | C | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+3061T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867628 | ||||||
chr6:143867668
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.28+3101A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867668 | ||||||
chr6:143867808
|
T | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.28+3241T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867808 | ||||||
chr6:143868006
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28+3439T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868006 | ||||||
chr6:143868095
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00673.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.28+3528A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868095 | ||||||
chr6:143868318
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.28+3751C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868318 | ||||||
chr6:143868335
|
A | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+3768A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868335 | ||||||
chr6:143868368
|
A | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+3801A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868368 | ||||||
chr6:143868375
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0322 | 3 | HG02109.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28+3808A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868375 | ||||||
chr6:143868423
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.28+3856G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868423 | ||||||
chr6:143868466
|
A | AC | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+3899_28+3900ins others(1): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868466 | ||||||
chr6:143868466
|
A | AT | 115 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 118 | HG00408.hp2 HG00423.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.28+3909dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143868466 | |||||
chr6:143868466
|
A | ATT | 34 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0106others(31): Show | 34 | HG00140.hp2 HG00673.hp1 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.28+3908_28+3909dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143868466 | |||||
chr6:143868581
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.28+4014C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868581 | ||||||
chr6:143868758
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28+4191T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868758 | ||||||
chr6:143869193
|
A | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0123others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.28+4626A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869193 | ||||||
chr6:143869208
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+4641C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869208 | ||||||
chr6:143869315
|
A | T | 1 | a0001c0001t0001g0032 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.28+4748A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869315 | ||||||
chr6:143869449
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.28+4882C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869449 | ||||||
chr6:143869535
|
ATAAGGCA others(3): Show |
A | 1 | a0001c0001t0001g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+4971_28+4980del others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143869535 | |||||
chr6:143869874
|
C | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0043others(64): Show | 69 | HG00099.hp1 HG00408.hp2 HG01123.hp1 others(66): Show |
intron_variant | MODIFIER | c.28+5307C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869874 | ||||||
chr6:143870100
|
A | G | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+5533A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870100 | ||||||
chr6:143870219
|
G | T | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.28+5652G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870219 | ||||||
chr6:143870357
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.28+5790C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870357 | ||||||
chr6:143870479
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+5912A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870479 | ||||||
chr6:143870568
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+6001A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870568 | ||||||
chr6:143870608
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+6041T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870608 | ||||||
chr6:143870803
|
C | T | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+6236C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870803 | ||||||
chr6:143870809
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(108): Show | 114 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(111): Show |
intron_variant | MODIFIER | c.28+6242C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870809 | ||||||
chr6:143870829
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.28+6262A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870829 | ||||||
chr6:143871072
|
A | T | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.28+6505A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871072 | ||||||
chr6:143871258
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.28+6691A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871258 | ||||||
chr6:143871271
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28+6704G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871271 | ||||||
chr6:143871450
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.28+6883G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871450 | ||||||
chr6:143871518
|
T | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(89): Show | 94 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.28+6951T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871518 | ||||||
chr6:143871592
|
C | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+7025C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871592 | ||||||
chr6:143871773
|
C | T | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+7206C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871773 | ||||||
chr6:143871779
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.28+7212A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871779 | ||||||
chr6:143871944
|
T | G | 13 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(10): Show | 13 | HG01261.hp1 HG01361.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.28+7377T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871944 | ||||||
chr6:143871969
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.28+7402G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871969 | ||||||
chr6:143872013
|
ACATCAGC others(14): Show |
A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.28+7449_28+7469del others(21): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143872013 | |||||
chr6:143872070
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.28+7503C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872070 | ||||||
chr6:143872216
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0044others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+7649C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872216 | ||||||
chr6:143872296
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0044others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+7729C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872296 | ||||||
chr6:143872338
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.28+7771A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872338 | ||||||
chr6:143872446
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.28+7879C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872446 | ||||||
chr6:143872480
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0153others(6): Show | 11 | HG00408.hp2 HG02071.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+7913G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872480 | ||||||
chr6:143872501
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.28+7934C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872501 | ||||||
chr6:143872555
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.28+7988G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872555 | ||||||
chr6:143872656
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.28+8089G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872656 | ||||||
chr6:143872668
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8101A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872668 | ||||||
chr6:143872673
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8106A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872673 | ||||||
chr6:143872680
|
A | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8113A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872680 | ||||||
chr6:143872683
|
A | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8116A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872683 | ||||||
chr6:143872695
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8128G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872695 | ||||||
chr6:143872810
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.28+8243G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872810 | ||||||
chr6:143872925
|
A | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01928.hp1 HG01934.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+8358A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872925 | ||||||
chr6:143872949
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.28+8382A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872949 | ||||||
chr6:143873097
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.28+8530A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873097 | ||||||
chr6:143873108
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 5 | HG01123.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+8541G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873108 | ||||||
chr6:143873184
|
A | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | NA18948.hp2 NA18957.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+8617A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873184 | ||||||
chr6:143873422
|
G | T | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.28+8855G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873422 | ||||||
chr6:143873458
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(86): Show | 91 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.28+8891C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873458 | ||||||
chr6:143873480
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 105 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.28+8913T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873480 | ||||||
chr6:143873552
|
T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8985T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873552 | ||||||
chr6:143873579
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+9012C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873579 | ||||||
chr6:143873772
|
A | G | 6 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.28+9205A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873772 | ||||||
chr6:143873812
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.28+9245C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873812 | ||||||
chr6:143873850
|
G | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+9283G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873850 | ||||||
chr6:143873973
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 105 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.28+9406C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873973 | ||||||
chr6:143874045
|
T | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.28+9478T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874045 | ||||||
chr6:143874130
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.28+9563T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874130 | ||||||
chr6:143874154
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.28+9587C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874154 | ||||||
chr6:143874192
|
CAA | C | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+9626_28+9627del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874192 | ||||||
chr6:143874246
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28+9679A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874246 | ||||||
chr6:143874313
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.28+9746T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874313 | ||||||
chr6:143874335
|
A | G | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.28+9768A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874335 | ||||||
chr6:143874348
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.28+9781C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874348 | ||||||
chr6:143874416
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28+9849G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874416 | ||||||
chr6:143874497
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.29-9807C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874497 | ||||||
chr6:143874587
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(86): Show | 91 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.29-9717T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874587 | ||||||
chr6:143874763
|
G | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-9541G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874763 | ||||||
chr6:143874800
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02055.hp1 HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-9504A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874800 | ||||||
chr6:143874808
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0322 | 3 | HG02109.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-9496A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874808 | ||||||
chr6:143874845
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-9459G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874845 | ||||||
chr6:143874891
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-9413G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874891 | ||||||
chr6:143874927
|
G | A | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(39): Show | 42 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.29-9377G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874927 | ||||||
chr6:143874945
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.29-9359G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874945 | ||||||
chr6:143874952
|
C | A | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.29-9352C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874952 | ||||||
chr6:143875005
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.29-9299G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875005 | ||||||
chr6:143875038
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.29-9266G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875038 | ||||||
chr6:143875053
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.29-9251G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875053 | ||||||
chr6:143875078
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-9226C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875078 | ||||||
chr6:143875086
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.29-9218G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875086 | ||||||
chr6:143875221
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.29-9083A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875221 | ||||||
chr6:143875316
|
TCTAAAGT others(3418): Show |
T | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(11): Show | 14 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-8983_29-5559del | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143875316 | |||||
chr6:143875576
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.29-8728C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875576 | ||||||
chr6:143875721
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.29-8583T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875721 | ||||||
chr6:143875769
|
T | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.29-8535T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875769 | ||||||
chr6:143875838
|
C | T | 2 | a0002c0002t0001g0024a0002c0002t0001g0025 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.29-8466C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875838 | ||||||
chr6:143875853
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-8451A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875853 | ||||||
chr6:143875868
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 171 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.29-8436C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875868 | ||||||
chr6:143875874
|
G | A | 1 | a0002c0002t0001g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.29-8430G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875874 | ||||||
chr6:143876175
|
C | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 90 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.29-8129C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876175 | ||||||
chr6:143876238
|
A | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.29-8066A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876238 | ||||||
chr6:143876265
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 90 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.29-8039A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876265 | ||||||
chr6:143876281
|
C | A | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-8023C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876281 | ||||||
chr6:143876339
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-7965A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876339 | ||||||
chr6:143876441
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-7863G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876441 | ||||||
chr6:143876444
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-7860T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876444 | ||||||
chr6:143876544
|
T | G | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-7760T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876544 | ||||||
chr6:143876605
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-7699G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876605 | ||||||
chr6:143876918
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.29-7386T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876918 | ||||||
chr6:143876941
|
T | TA | 4 | a0001c0001t0001g0004a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 5 | HG01123.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-7361dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143876941 | |||||
chr6:143876952
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.29-7352G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876952 | ||||||
chr6:143877005
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.29-7299G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877005 | ||||||
chr6:143877044
|
A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-7260A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877044 | ||||||
chr6:143877140
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-7164G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877140 | ||||||
chr6:143877272
|
C | CT | 36 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0058others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.29-7005dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877272
|
C | CTT | 46 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 47 | HG01123.hp1 HG01243.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.29-7006_29-7005dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877272
|
C | CTTT | 29 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0049others(26): Show | 30 | HG00408.hp2 HG01358.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.29-7007_29-7005dup others(3): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877272
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-7014_29-7005dup others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877272
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.29-7015_29-7005dup others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877272
|
CT | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0026others(27): Show | 30 | HG01099.hp1 HG01168.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.29-7005delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877272
|
CTTTTTTT others(1): Show |
C | 34 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 35 | HG00140.hp2 HG00673.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.29-7012_29-7005del others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | |||||
chr6:143877342
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-6962G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877342 | ||||||
chr6:143877352
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 78 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.29-6952A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877352 | ||||||
chr6:143877361
|
A | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 78 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.29-6943A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877361 | ||||||
chr6:143877511
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 78 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.29-6793A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877511 | ||||||
chr6:143877562
|
C | T | 11 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-6742C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877562 | ||||||
chr6:143877576
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-6728C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877576 | ||||||
chr6:143878075
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-6229C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878075 | ||||||
chr6:143878174
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-6130C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878174 | ||||||
chr6:143878345
|
G | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(1): Show | 4 | NA18956.hp1 NA18964.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-5959G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878345 | ||||||
chr6:143878393
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0120others(32): Show | 35 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.29-5911G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878393 | ||||||
chr6:143878479
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.29-5825A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878479 | ||||||
chr6:143878483
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.29-5821C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878483 | ||||||
chr6:143878514
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 92 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.29-5790T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878514 | ||||||
chr6:143878940
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.29-5364C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878940 | ||||||
chr6:143879018
|
G | A | 10 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(7): Show | 10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-5286G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879018 | ||||||
chr6:143879033
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-5271C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879033 | ||||||
chr6:143879095
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-5209G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879095 | ||||||
chr6:143879112
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(11): Show | 14 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-5192C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879112 | ||||||
chr6:143879674
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-4630C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879674 | ||||||
chr6:143879791
|
G | GT | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(180): Show | 187 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.29-4500dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879791 | |||||
chr6:143879824
|
A | AT | 25 | a0001c0001t0001g0012a0001c0001t0001g0107a0001c0001t0001g0108others(22): Show | 25 | HG00733.hp1 HG00738.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.29-4455dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | |||||
chr6:143879824
|
A | ATTTT | 8 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-4458_29-4455dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | |||||
chr6:143879824
|
A | ATTTTT | 21 | a0001c0001t0001g0014a0001c0001t0001g0123a0001c0001t0001g0133others(18): Show | 21 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-4459_29-4455dup others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | |||||
chr6:143879824
|
AT | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(88): Show | 94 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.29-4455delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | |||||
chr6:143879861
|
T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.29-4443T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879861 | ||||||
chr6:143879878
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.29-4426A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879878 | ||||||
chr6:143880002
|
T | G | 1 | a0003c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.29-4302T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880002 | ||||||
chr6:143880016
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29-4288A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880016 | ||||||
chr6:143880236
|
G | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0026others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.29-4068G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880236 | ||||||
chr6:143880565
|
TA | T | 5 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(2): Show | 5 | HG02683.hp2 HG03239.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-3734delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143880565 | |||||
chr6:143880687
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-3617G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880687 | ||||||
chr6:143880828
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.29-3476C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880828 | ||||||
chr6:143880993
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.29-3311C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880993 | ||||||
chr6:143881054
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.29-3250C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881054 | ||||||
chr6:143881111
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.29-3193T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881111 | ||||||
chr6:143881133
|
A | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 50 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.29-3171A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881133 | ||||||
chr6:143881166
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-3138G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881166 | ||||||
chr6:143881302
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0107others(11): Show | 14 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-3002A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881302 | ||||||
chr6:143881498
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 3 | HG02486.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.29-2806C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881498 | ||||||
chr6:143881550
|
C | CA | 48 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0028others(45): Show | 49 | HG00423.hp1 HG00423.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.29-2727dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | |||||
chr6:143881550
|
C | CAAAA | 7 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0309others(4): Show | 7 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-2730_29-2727dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | |||||
chr6:143881550
|
CA | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0086a0001c0001t0001g0177others(3): Show | 6 | HG00609.hp1 HG01168.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-2727delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | |||||
chr6:143881550
|
CAAAAAA | C | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01081.hp2 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-2732_29-2727del others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | |||||
chr6:143881550
|
CAAAAAAA | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0120others(36): Show | 39 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.29-2733_29-2727del others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | |||||
chr6:143881570
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-2734A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881570 | ||||||
chr6:143881574
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.29-2730A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881574 | ||||||
chr6:143881608
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.29-2696A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881608 | ||||||
chr6:143881714
|
T | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0321 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.29-2590T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881714 | ||||||
chr6:143881864
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.29-2440T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881864 | ||||||
chr6:143881882
|
T | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0193 | 3 | NA18963.hp1 NA18984.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.29-2422T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881882 | ||||||
chr6:143881968
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-2336G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881968 | ||||||
chr6:143882046
|
G | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.29-2258G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882046 | ||||||
chr6:143882221
|
T | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 50 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.29-2083T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882221 | ||||||
chr6:143882250
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.29-2054G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882250 | ||||||
chr6:143882325
|
T | TTA | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0314others(2): Show | 5 | HG01192.hp1 HG02109.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1975_29-1974dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882325 | |||||
chr6:143882329
|
A | AT | 21 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0064others(18): Show | 23 | HG00408.hp2 HG01952.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-1969dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882329 | |||||
chr6:143882329
|
ATT | A | 8 | a0001c0001t0001g0182a0001c0001t0001g0190a0001c0001t0001g0209others(5): Show | 8 | HG01433.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-1970_29-1969del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882329 | |||||
chr6:143882331
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(91): Show | 96 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.29-1973T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882331 | ||||||
chr6:143882332
|
T | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.29-1972T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882332 | ||||||
chr6:143882332
|
T | TTA | 7 | a0001c0001t0001g0198a0001c0001t0001g0261a0001c0001t0001g0273others(4): Show | 7 | HG02027.hp2 HG02080.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATA | 11 | a0001c0001t0001g0055a0001c0001t0001g0179a0001c0001t0001g0184others(8): Show | 11 | HG00438.hp1 HG01884.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATA | 5 | a0001c0001t0001g0160a0001c0001t0001g0187a0001c0001t0001g0195others(2): Show | 5 | HG00423.hp1 NA18949.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0001g0245a0001c0001t0001g0257a0001c0001t0001g0300 | 3 | HG02040.hp1 HG03516.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0256 | 2 | HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.29-1971_29-1970ins others(14): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0001g0194 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.29-1971_29-1970ins others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0315 | 2 | HG01261.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0301 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.29-1971_29-1970ins others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882332
|
TTTTATAT others(13): Show |
T | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.29-1970_29-1951del others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | |||||
chr6:143882333
|
T | A | 5 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1971T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882333 | ||||||
chr6:143882334
|
T | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.29-1970T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882334 | ||||||
chr6:143882334
|
T | TATATATA others(2): Show |
3 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0093 | 3 | HG04204.hp2 NA19068.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.29-1970_29-1969ins others(9): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882334 | ||||||
chr6:143882334
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0092 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.29-1970_29-1969ins others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882334 | ||||||
chr6:143882334
|
T | TTA | 7 | a0001c0001t0001g0119a0001c0001t0001g0159a0001c0001t0001g0183others(4): Show | 7 | HG01106.hp2 HG02630.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-1936_29-1935dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATA | 8 | a0001c0001t0001g0038a0001c0001t0001g0135a0001c0001t0001g0191others(5): Show | 8 | HG01934.hp1 HG01943.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-1938_29-1935dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATA | 9 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(6): Show | 10 | HG01106.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-1940_29-1935dup others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0181a0001c0001t0001g0210others(1): Show | 4 | HG03579.hp1 HG04184.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-1942_29-1935dup others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(3): Show |
9 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0031others(6): Show | 9 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.29-1944_29-1935dup others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(5): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0116others(1): Show | 4 | HG01081.hp2 HG01258.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-1946_29-1935dup others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0046a0002c0002t0001g0025 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.29-1950_29-1935dup others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(11): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0107others(5): Show | 8 | HG01884.hp1 HG02602.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1952_29-1935dup others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.29-1954_29-1935dup others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(15): Show |
8 | a0001c0001t0001g0012a0001c0001t0001g0110a0001c0001t0001g0112others(5): Show | 8 | HG02145.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1956_29-1935dup others(22): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(17): Show |
3 | a0001c0001t0001g0128a0001c0001t0001g0297a0002c0002t0001g0021 | 3 | HG02717.hp1 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.29-1958_29-1935dup others(24): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(19): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0296others(2): Show | 5 | HG00733.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1960_29-1935dup others(26): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.29-1962_29-1935dup others(28): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(23): Show |
2 | a0001c0001t0001g0026a0002c0002t0001g0018 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29-1964_29-1935dup others(30): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(27): Show |
2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.29-1968_29-1935dup others(34): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(14): Show |
2 | a0003c0003t0001g0034a0003c0003t0001g0035 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.29-1963_29-1962ins others(21): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTATATAT others(26): Show |
1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-1963_29-1962ins others(33): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTA | 17 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0053others(14): Show | 17 | HG00099.hp1 HG00738.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(3): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTATATA | 7 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0072others(4): Show | 7 | HG01168.hp1 HG04115.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTATATA others(2): Show |
7 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0069others(4): Show | 7 | HG01243.hp2 HG02080.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(9): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTATATA others(4): Show |
5 | a0001c0001t0001g0068a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18942.hp1 NA18956.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTATATA others(6): Show |
1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(13): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTATATA others(12): Show |
1 | a0001c0001t0001g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(19): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTTATAT others(9): Show |
1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTTATAT others(11): Show |
1 | a0001c0001t0001g0122 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTTATAT others(15): Show |
1 | a0001c0001t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(22): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
T | TTTTATAT others(17): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(24): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
TTA | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0130others(53): Show | 57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.29-1936_29-1935del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882334
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.29-1952_29-1935del others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | |||||
chr6:143882335
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.29-1968_29-1956del others(13): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882335 | ||||||
chr6:143882336
|
A | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 5 | HG00408.hp2 HG02071.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-1968A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882336 | ||||||
chr6:143882340
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-1964A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882340 | ||||||
chr6:143882369
|
T | TATATATA others(10): Show |
1 | a0001c0001t0001g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.29-1935_29-1934ins others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882369 | ||||||
chr6:143882467
|
A | G | 10 | a0001c0001t0001g0176a0001c0001t0001g0208a0001c0001t0001g0241others(7): Show | 10 | HG00438.hp1 HG02027.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.29-1837A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882467 | ||||||
chr6:143882504
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-1800T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882504 | ||||||
chr6:143882640
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0303others(11): Show | 15 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.29-1664A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882640 | ||||||
chr6:143882905
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29-1399C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882905 | ||||||
chr6:143883051
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0120others(35): Show | 38 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.29-1253A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883051 | ||||||
chr6:143883186
|
C | T | 60 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0160others(57): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.29-1118C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883186 | ||||||
chr6:143883231
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.29-1073A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883231 | ||||||
chr6:143883258
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0044others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1046C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883258 | ||||||
chr6:143883265
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(65): Show | 70 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.29-1039T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883265 | ||||||
chr6:143883473
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(38): Show | 42 | HG00733.hp1 HG01106.hp1 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.29-831T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883473 | ||||||
chr6:143883538
|
C | CT | 9 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(6): Show | 9 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-759dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143883538 | |||||
chr6:143883679
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.29-625A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883679 | ||||||
chr6:143883781
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.29-523A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883781 | ||||||
chr6:143883942
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29-362A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883942 | ||||||
chr6:143884058
|
A | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.29-246A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143884058 | ||||||
chr6:143884454
|
A | G | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+89A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884454 | ||||||
chr6:143884558
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.90+193C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884558 | ||||||
chr6:143884622
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0172a0001c0001t0001g0177others(10): Show | 14 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.90+257C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884622 | ||||||
chr6:143884644
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(26): Show | 30 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.90+279A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884644 | ||||||
chr6:143884733
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+368A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884733 | ||||||
chr6:143884816
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.90+451G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884816 | ||||||
chr6:143884891
|
A | G | 1 | a0003c0003t0001g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.90+526A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884891 | ||||||
chr6:143885002
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.90+637G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885002 | ||||||
chr6:143885158
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.90+793G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885158 | ||||||
chr6:143885299
|
C | CCACCAGG others(10): Show |
1 | a0001c0001t0001g0321 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.91-727_91-726insGG others(15): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 143885299 | |||||
chr6:143885306
|
T | A | 1 | a0001c0001t0001g0172 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91-726T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885306 | ||||||
chr6:143885328
|
A | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 63 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-704A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885328 | ||||||
chr6:143885363
|
C | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0107a0001c0001t0001g0108others(9): Show | 12 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.91-669C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885363 | ||||||
chr6:143885517
|
C | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.91-515C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885517 | ||||||
chr6:143885540
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.91-492T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885540 | ||||||
chr6:143885552
|
T | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 26 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.91-480T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885552 | ||||||
chr6:143885634
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.91-398T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885634 | ||||||
chr6:143885713
|
A | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.91-319A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885713 | ||||||
chr6:143885714
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0241a0001c0001t0001g0251 | 3 | NA18951.hp2 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.91-318A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885714 | ||||||
chr6:143885742
|
GGAGTA | G | 12 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-289_91-285delGA others(3): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885742 | ||||||
chr6:143886394
|
A | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0046others(68): Show | 73 | HG00408.hp2 HG00738.hp2 HG01123.hp1 others(70): Show |
intron_variant | MODIFIER | c.210+243A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | chr6 | 143886394 | ||||||
chr6:143886425
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.211-258A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | chr6 | 143886425 | ||||||
chr6:143886460
|
A | AT | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.211-218dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 143886460 | |||||
chr6:143886526
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.211-157T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | chr6 | 143886526 | ||||||
chr6:143886975
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.349+154A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143886975 | ||||||
chr6:143887042
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.349+221A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887042 | ||||||
chr6:143887216
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.349+395A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887216 | ||||||
chr6:143887275
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.349+454T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887275 | ||||||
chr6:143887517
|
T | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0044others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+696T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887517 | ||||||
chr6:143887608
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+787C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887608 | ||||||
chr6:143887716
|
T | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0107a0001c0001t0001g0108others(21): Show | 24 | HG00733.hp1 HG01099.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.349+895T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887716 | ||||||
chr6:143887900
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1079C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887900 | ||||||
chr6:143888251
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.349+1430A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888251 | ||||||
chr6:143888367
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(60): Show | 64 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.349+1546T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888367 | ||||||
chr6:143888368
|
G | A | 12 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+1547G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888368 | ||||||
chr6:143888493
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.349+1672A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888493 | ||||||
chr6:143888527
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349+1706A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888527 | ||||||
chr6:143888545
|
AT | A | 4 | a0001c0001t0001g0320a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1727delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143888545 | |||||
chr6:143888550
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.349+1729C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888550 | ||||||
chr6:143889065
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.349+2244A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889065 | ||||||
chr6:143889106
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0123others(32): Show | 35 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.349+2285A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889106 | ||||||
chr6:143889182
|
CT | C | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+2362delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889182 | ||||||
chr6:143889216
|
T | C | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349+2395T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889216 | ||||||
chr6:143889521
|
A | AG | 25 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 26 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.349+2701dupG | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143889521 | |||||
chr6:143889562
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.349+2741G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889562 | ||||||
chr6:143889601
|
A | G | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+2780A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889601 | ||||||
chr6:143889721
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.349+2900A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889721 | ||||||
chr6:143889778
|
A | T | 4 | a0001c0001t0001g0320a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+2957A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889778 | ||||||
chr6:143889834
|
C | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0241a0001c0001t0001g0251 | 3 | NA18951.hp2 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.349+3013C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889834 | ||||||
chr6:143889931
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0101 | 2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.349+3110A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889931 | ||||||
chr6:143890058
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.349+3237C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890058 | ||||||
chr6:143890135
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.349+3314G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890135 | ||||||
chr6:143890398
|
C | CA | 11 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0001g0112others(8): Show | 11 | HG02074.hp1 HG02145.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+3594dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143890398 | |||||
chr6:143890398
|
CA | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(32): Show | 36 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.349+3594delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143890398 | |||||
chr6:143890493
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0286 | 2 | NA19075.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.349+3672T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890493 | ||||||
chr6:143890706
|
G | T | 4 | a0001c0001t0001g0320a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+3885G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890706 | ||||||
chr6:143890855
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.349+4034C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890855 | ||||||
chr6:143890912
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.349+4091G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890912 | ||||||
chr6:143890926
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG03017.hp2 HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.349+4105G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890926 | ||||||
chr6:143891130
|
C | CA | 27 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0001t0001g0107others(24): Show | 27 | HG00639.hp1 HG00733.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+4324dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891130 | |||||
chr6:143891130
|
CA | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.349+4324delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891130 | |||||
chr6:143891251
|
A | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.349+4430A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891251 | ||||||
chr6:143891356
|
A | G | 2 | a0003c0003t0001g0034a0003c0003t0001g0035 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349+4535A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891356 | ||||||
chr6:143891438
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+4617C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891438 | ||||||
chr6:143891466
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.349+4645C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891466 | ||||||
chr6:143891686
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.349+4865T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891686 | ||||||
chr6:143891693
|
CA | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.349+4887delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891693 | |||||
chr6:143891705
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349+4884A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891705 | ||||||
chr6:143891876
|
A | AT | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(35): Show | 39 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.349+5056dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891876 | |||||
chr6:143892297
|
C | CT | 16 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 17 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+5492dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143892297 | |||||
chr6:143892297
|
CT | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0087others(15): Show | 18 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+5492delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143892297 | |||||
chr6:143892367
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0236 | 3 | NA18983.hp2 NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.349+5546C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892367 | ||||||
chr6:143892734
|
A | C | 2 | a0003c0003t0001g0034a0003c0003t0001g0035 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-5818A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892734 | ||||||
chr6:143892905
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.350-5647T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892905 | ||||||
chr6:143892906
|
A | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0107a0001c0001t0001g0108others(7): Show | 10 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-5646A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892906 | ||||||
chr6:143893002
|
GA | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG01884.hp1 HG01978.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.350-5539delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143893002 | |||||
chr6:143893002
|
GAA | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-5540_350-5539d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143893002 | |||||
chr6:143893028
|
A | T | 6 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-5524A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893028 | ||||||
chr6:143893048
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-5504C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893048 | ||||||
chr6:143893337
|
G | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0107a0001c0001t0001g0108others(9): Show | 12 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-5215G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893337 | ||||||
chr6:143893340
|
G | A | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-5212G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893340 | ||||||
chr6:143893353
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-5199C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893353 | ||||||
chr6:143893355
|
G | A | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-5197G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893355 | ||||||
chr6:143893380
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-5172C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893380 | ||||||
chr6:143893417
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0101 | 2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.350-5135A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893417 | ||||||
chr6:143893417
|
A | T | 1 | a0001c0001t0001g0291 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.350-5135A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893417 | ||||||
chr6:143893422
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.350-5130G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893422 | ||||||
chr6:143893443
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.350-5109C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893443 | ||||||
chr6:143893721
|
C | G | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-4831C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893721 | ||||||
chr6:143893780
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.350-4772A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893780 | ||||||
chr6:143893787
|
C | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0059others(33): Show | 36 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.350-4765C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893787 | ||||||
chr6:143893832
|
A | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0118others(4): Show | 7 | HG01433.hp1 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-4720A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893832 | ||||||
chr6:143893832
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-4720A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893832 | ||||||
chr6:143893925
|
A | C | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02723.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.350-4627A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893925 | ||||||
chr6:143893950
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.350-4602T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893950 | ||||||
chr6:143893954
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-4598G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893954 | ||||||
chr6:143893978
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.350-4574G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893978 | ||||||
chr6:143893992
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-4560G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893992 | ||||||
chr6:143894166
|
TAAAC | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-4384_350-4381d others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143894166 | |||||
chr6:143894278
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.350-4274T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894278 | ||||||
chr6:143894362
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-4190T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894362 | ||||||
chr6:143894398
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-4154T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894398 | ||||||
chr6:143894418
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.350-4134G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894418 | ||||||
chr6:143894585
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.350-3967C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894585 | ||||||
chr6:143894978
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-3574A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894978 | ||||||
chr6:143895004
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-3548C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895004 | ||||||
chr6:143895076
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.350-3476C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895076 | ||||||
chr6:143895077
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.350-3475A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895077 | ||||||
chr6:143895079
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-3473G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895079 | ||||||
chr6:143895311
|
C | T | 6 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0114others(3): Show | 6 | HG01928.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3241C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895311 | ||||||
chr6:143895408
|
A | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 61 | HG01099.hp1 HG01106.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.350-3144A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895408 | ||||||
chr6:143895414
|
C | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(40): Show | 43 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.350-3138C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895414 | ||||||
chr6:143895458
|
C | T | 6 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0078others(3): Show | 6 | NA18959.hp1 NA18979.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-3094C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895458 | ||||||
chr6:143895608
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-2944T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895608 | ||||||
chr6:143895708
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-2844A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895708 | ||||||
chr6:143895726
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-2826A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895726 | ||||||
chr6:143895741
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-2811T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895741 | ||||||
chr6:143895836
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 59 | HG01106.hp1 HG01192.hp1 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.350-2716G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895836 | ||||||
chr6:143895942
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-2610G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895942 | ||||||
chr6:143896050
|
A | G | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-2502A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896050 | ||||||
chr6:143896068
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-2484G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896068 | ||||||
chr6:143896100
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-2452C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896100 | ||||||
chr6:143896614
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-1938G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896614 | ||||||
chr6:143896657
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 59 | HG01106.hp1 HG01192.hp1 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.350-1895T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896657 | ||||||
chr6:143896765
|
A | G | 10 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(7): Show | 10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1787A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896765 | ||||||
chr6:143897001
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.350-1551G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897001 | ||||||
chr6:143897090
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.350-1462C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897090 | ||||||
chr6:143897190
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.350-1362C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897190 | ||||||
chr6:143897457
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.350-1095C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897457 | ||||||
chr6:143897475
|
T | G | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-1077T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897475 | ||||||
chr6:143897505
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.350-1047T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897505 | ||||||
chr6:143897510
|
T | A | 11 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0110others(8): Show | 11 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-1042T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897510 | ||||||
chr6:143897667
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-885T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897667 | ||||||
chr6:143897842
|
C | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-710C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897842 | ||||||
chr6:143897926
|
C | A | 12 | a0001c0001t0001g0128a0002c0002t0001g0015a0002c0002t0001g0016others(9): Show | 12 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-626C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897926 | ||||||
chr6:143897958
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0044others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-594A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897958 | ||||||
chr6:143898103
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-449C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143898103 | ||||||
chr6:143898233
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.350-319G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143898233 | ||||||
chr6:143898539
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.350-13T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143898539 | ||||||
chr6:143899127
|
A | G | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.489+436A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899127 | ||||||
chr6:143899267
|
C | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0056others(50): Show | 54 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.489+576C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899267 | ||||||
chr6:143899398
|
CAG | C | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0209others(2): Show | 5 | HG01433.hp1 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+708_489+709del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899398 | ||||||
chr6:143899492
|
C | T | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+801C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899492 | ||||||
chr6:143899532
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.489+841C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899532 | ||||||
chr6:143899774
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489+1083G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899774 | ||||||
chr6:143900070
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489+1379G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900070 | ||||||
chr6:143900092
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.489+1401C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900092 | ||||||
chr6:143900222
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+1531T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900222 | ||||||
chr6:143900262
|
G | C | 4 | a0001c0001t0001g0320a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1571G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900262 | ||||||
chr6:143900390
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(120): Show | 125 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.489+1714dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143900390 | |||||
chr6:143900433
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+1742G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900433 | ||||||
chr6:143900556
|
GACAGGTC others(8): Show |
G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.489+1893_489+1907d others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143900556 | |||||
chr6:143900597
|
G | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1906G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900597 | ||||||
chr6:143900619
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+1928G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900619 | ||||||
chr6:143900795
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0272 | 3 | HG00099.hp2 HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.489+2104G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900795 | ||||||
chr6:143900864
|
A | T | 15 | a0001c0001t0001g0320a0002c0002t0001g0015a0002c0002t0001g0016others(12): Show | 15 | HG02109.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2173A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900864 | ||||||
chr6:143900874
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.490-2170T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900874 | ||||||
chr6:143900925
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2119G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900925 | ||||||
chr6:143900941
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.490-2103C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900941 | ||||||
chr6:143900942
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.490-2102G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900942 | ||||||
chr6:143900956
|
A | G | 10 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 10 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-2088A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900956 | ||||||
chr6:143900981
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 192 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.490-2063A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900981 | ||||||
chr6:143901048
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 32 | HG00733.hp1 HG01192.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.490-1996A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901048 | ||||||
chr6:143901081
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-1963C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901081 | ||||||
chr6:143901177
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.490-1867G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901177 | ||||||
chr6:143901250
|
C | CT | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(83): Show | 87 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.490-1767dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | |||||
chr6:143901250
|
C | CTT | 32 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0047others(29): Show | 32 | HG00733.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-1768_490-1767d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | |||||
chr6:143901250
|
C | CTTT | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0044others(9): Show | 12 | HG01258.hp1 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-1769_490-1767d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | |||||
chr6:143901250
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0196 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-1780_490-1767d others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | |||||
chr6:143901250
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.490-1781_490-1767d others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | |||||
chr6:143901317
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.490-1727T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901317 | ||||||
chr6:143901424
|
T | C | 11 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(8): Show | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-1620T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901424 | ||||||
chr6:143901550
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-1494G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901550 | ||||||
chr6:143901563
|
G | A | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.490-1481G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901563 | ||||||
chr6:143901793
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG01192.hp1 HG01258.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.490-1251G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901793 | ||||||
chr6:143901884
|
G | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG01192.hp1 HG01258.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.490-1160G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901884 | ||||||
chr6:143902477
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.490-567C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902477 | ||||||
chr6:143902526
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.490-518A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902526 | ||||||
chr6:143902707
|
T | A | 9 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0110others(6): Show | 9 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-337T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902707 | ||||||
chr6:143902750
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.490-294T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902750 | ||||||
chr6:143902772
|
T | C | 10 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(7): Show | 10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-272T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902772 | ||||||
chr6:143902889
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.490-155G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902889 | ||||||
chr6:143902947
|
T | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | NA18747.hp2 NA18951.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-97T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902947 | ||||||
chr6:143902988
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.490-56A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902988 | ||||||
chr6:143903031
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.490-13T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143903031 | ||||||
chr6:143903175
|
T | G | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(29): Show | 32 | HG01192.hp1 HG01884.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.598+23T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903175 | ||||||
chr6:143903334
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01943.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.598+182A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903334 | ||||||
chr6:143903444
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+292C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903444 | ||||||
chr6:143903486
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.598+334T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903486 | ||||||
chr6:143903587
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.598+435A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903587 | ||||||
chr6:143903743
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0159 | 2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.598+591C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903743 | ||||||
chr6:143904224
|
A | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+1072A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904224 | ||||||
chr6:143904474
|
A | G | 9 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+1322A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904474 | ||||||
chr6:143904533
|
T | A | 1 | a0001c0001t0001g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.598+1381T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904533 | ||||||
chr6:143904543
|
G | A | 9 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+1391G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904543 | ||||||
chr6:143904633
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+1481T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904633 | ||||||
chr6:143904727
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0256 | 3 | HG01109.hp1 HG01123.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.598+1575G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904727 | ||||||
chr6:143904745
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.598+1593G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904745 | ||||||
chr6:143904950
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.598+1798C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904950 | ||||||
chr6:143905166
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0248others(2): Show | 5 | NA18940.hp2 NA18965.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+2014A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905166 | ||||||
chr6:143905373
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.598+2221A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905373 | ||||||
chr6:143905570
|
G | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0190a0001c0001t0001g0196others(2): Show | 5 | HG02486.hp1 HG04184.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+2418G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905570 | ||||||
chr6:143905787
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+2635G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905787 | ||||||
chr6:143905878
|
C | T | 7 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0309others(4): Show | 7 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.598+2726C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905878 | ||||||
chr6:143905994
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.598+2842A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905994 | ||||||
chr6:143906091
|
G | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(2): Show | 5 | HG03490.hp1 HG03710.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+2939G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906091 | ||||||
chr6:143906160
|
C | T | 2 | a0001c0001t0001g0030a0004c0004t0001g0057 | 2 | NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.598+3008C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906160 | ||||||
chr6:143906340
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+3188C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906340 | ||||||
chr6:143906362
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.598+3210A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906362 | ||||||
chr6:143906367
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+3215A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906367 | ||||||
chr6:143906370
|
G | T | 9 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+3218G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906370 | ||||||
chr6:143906424
|
T | G | 1 | a0001c0001t0001g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.598+3272T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906424 | ||||||
chr6:143906424
|
TTTTTAA | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(5): Show | 8 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+3289_598+3294d others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143906424 | |||||
chr6:143906683
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(74): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.598+3531A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906683 | ||||||
chr6:143906747
|
CT | C | 136 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.598+3609delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143906747 | |||||
chr6:143906747
|
CTT | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+3608_598+3609d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143906747 | |||||
chr6:143906748
|
T | A | 1 | a0001c0001t0001g0275 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.598+3596T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906748 | ||||||
chr6:143906818
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0037others(51): Show | 55 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.598+3666A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906818 | ||||||
chr6:143907091
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+3939T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907091 | ||||||
chr6:143907234
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.598+4082A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907234 | ||||||
chr6:143907515
|
A | C | 2 | a0003c0003t0001g0034a0003c0003t0001g0035 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+4363A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907515 | ||||||
chr6:143907517
|
T | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0207 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.598+4365T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907517 | ||||||
chr6:143907675
|
T | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 217 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.598+4523T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907675 | ||||||
chr6:143907895
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0240a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+4743T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907895 | ||||||
chr6:143908252
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+5100T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908252 | ||||||
chr6:143908253
|
A | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0116others(20): Show | 23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.598+5101A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908253 | ||||||
chr6:143908291
|
A | G | 5 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0218others(2): Show | 5 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+5139A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908291 | ||||||
chr6:143908292
|
G | GT | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.598+5146dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143908292 | |||||
chr6:143908320
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(74): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.598+5168A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908320 | ||||||
chr6:143908347
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.598+5195A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908347 | ||||||
chr6:143908393
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.598+5241T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908393 | ||||||
chr6:143908408
|
G | A | 13 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+5256G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908408 | ||||||
chr6:143908465
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.598+5313A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908465 | ||||||
chr6:143908570
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598+5418C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908570 | ||||||
chr6:143908779
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+5627G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908779 | ||||||
chr6:143908811
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.598+5659A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908811 | ||||||
chr6:143909285
|
T | A | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+6133T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909285 | ||||||
chr6:143909382
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.598+6230G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909382 | ||||||
chr6:143909421
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+6269G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909421 | ||||||
chr6:143909422
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+6270G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909422 | ||||||
chr6:143909498
|
T | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.598+6346T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909498 | ||||||
chr6:143909530
|
C | CT | 34 | a0001c0001t0001g0048a0001c0001t0001g0061a0001c0001t0001g0107others(31): Show | 34 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(31): Show |
intron_variant | MODIFIER | c.598+6395dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143909530 | |||||
chr6:143909530
|
CT | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 21 | HG01081.hp2 HG01168.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.598+6395delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143909530 | |||||
chr6:143909547
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.598+6395T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909547 | ||||||
chr6:143909666
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.598+6514A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909666 | ||||||
chr6:143909689
|
A | G | 8 | a0001c0001t0001g0188a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+6537A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909689 | ||||||
chr6:143909695
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.598+6543A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909695 | ||||||
chr6:143909794
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598+6642C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909794 | ||||||
chr6:143910066
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+6914C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910066 | ||||||
chr6:143910367
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.598+7215G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910367 | ||||||
chr6:143910419
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.598+7267C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910419 | ||||||
chr6:143910420
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598+7268A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910420 | ||||||
chr6:143910428
|
G | T | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+7276G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910428 | ||||||
chr6:143910499
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.598+7347A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910499 | ||||||
chr6:143910739
|
G | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+7587G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910739 | ||||||
chr6:143910894
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.598+7742G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910894 | ||||||
chr6:143910992
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.598+7840A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910992 | ||||||
chr6:143911300
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+8148G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143911300 | ||||||
chr6:143911718
|
A | G | 1 | a0003c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.598+8566A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143911718 | ||||||
chr6:143911826
|
T | C | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+8674T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143911826 | ||||||
chr6:143912059
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0240a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+8907C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912059 | ||||||
chr6:143912091
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0240a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+8939T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912091 | ||||||
chr6:143912097
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598+8945G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912097 | ||||||
chr6:143912228
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG03927.hp1 NA18952.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.598+9076G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912228 | ||||||
chr6:143912374
|
A | G | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+9222A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912374 | ||||||
chr6:143912521
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0256 | 4 | HG01109.hp1 HG01123.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+9369T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912521 | ||||||
chr6:143912693
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0262 | 2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.598+9541C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912693 | ||||||
chr6:143912804
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+9652C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912804 | ||||||
chr6:143913052
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.598+9900G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913052 | ||||||
chr6:143913229
|
T | TACC | 6 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0070others(3): Show | 6 | HG02083.hp1 HG02083.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+10078_598+1008 others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143913229 | |||||
chr6:143913422
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+10270G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913422 | ||||||
chr6:143913557
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+10405C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913557 | ||||||
chr6:143913651
|
T | A | 1 | a0001c0001t0001g0317 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.598+10499T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913651 | ||||||
chr6:143913756
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+10604T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913756 | ||||||
chr6:143913763
|
T | C | 16 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0160others(13): Show | 16 | HG01261.hp1 HG01361.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.598+10611T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913763 | ||||||
chr6:143913829
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+10677G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913829 | ||||||
chr6:143913881
|
C | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+10729C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913881 | ||||||
chr6:143913937
|
T | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+10785T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913937 | ||||||
chr6:143914000
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+10848A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914000 | ||||||
chr6:143914092
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.598+10940C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914092 | ||||||
chr6:143914150
|
G | A | 10 | a0001c0001t0001g0140a0002c0002t0001g0015a0002c0002t0001g0016others(7): Show | 10 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+10998G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914150 | ||||||
chr6:143914411
|
A | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+11259A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914411 | ||||||
chr6:143914493
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.598+11341G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914493 | ||||||
chr6:143914563
|
A | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.598+11411A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914563 | ||||||
chr6:143914773
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598+11621C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914773 | ||||||
chr6:143915132
|
C | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0116others(27): Show | 30 | HG00558.hp1 HG01081.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.598+11980C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915132 | ||||||
chr6:143915203
|
A | G | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+12051A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915203 | ||||||
chr6:143915356
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.598+12204A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915356 | ||||||
chr6:143915401
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.598+12249C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915401 | ||||||
chr6:143915444
|
G | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+12292G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915444 | ||||||
chr6:143915454
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598+12302C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915454 | ||||||
chr6:143915461
|
A | G | 1 | a0003c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.598+12309A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915461 | ||||||
chr6:143915486
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+12334A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915486 | ||||||
chr6:143915593
|
T | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(5): Show | 8 | HG03486.hp2 NA19003.hp2 NA19011.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+12441T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915593 | ||||||
chr6:143915728
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18942.hp1 NA18956.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+12576G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915728 | ||||||
chr6:143915819
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.598+12667A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915819 | ||||||
chr6:143916084
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0258 | 2 | HG02080.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.598+12932G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916084 | ||||||
chr6:143916239
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+13087C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916239 | ||||||
chr6:143916260
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+13108G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916260 | ||||||
chr6:143916340
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.598+13188A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916340 | ||||||
chr6:143916413
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.598+13261G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916413 | ||||||
chr6:143916478
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(74): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.598+13326C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916478 | ||||||
chr6:143916540
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0134others(3): Show | 6 | HG01258.hp1 HG02257.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+13388G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916540 | ||||||
chr6:143916750
|
G | T | 8 | a0001c0001t0001g0188a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+13598G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916750 | ||||||
chr6:143916942
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+13790T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916942 | ||||||
chr6:143917054
|
T | C | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598+13902T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917054 | ||||||
chr6:143917376
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.598+14224A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917376 | ||||||
chr6:143917385
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(111): Show | 115 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.598+14233G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917385 | ||||||
chr6:143917595
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.598+14443A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917595 | ||||||
chr6:143917636
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+14484C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917636 | ||||||
chr6:143917644
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0240a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+14492T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917644 | ||||||
chr6:143917735
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+14583T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917735 | ||||||
chr6:143917857
|
G | A | 13 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0001g0112others(10): Show | 13 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+14705G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917857 | ||||||
chr6:143917929
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0130a0001c0001t0001g0132others(11): Show | 14 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(11): Show |
intron_variant | MODIFIER | c.598+14777G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917929 | ||||||
chr6:143918169
|
C | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 74 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.598+15017C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918169 | ||||||
chr6:143918200
|
T | TA | 91 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(88): Show | 93 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.598+15048_598+1504 others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918200 | ||||||
chr6:143918209
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.598+15057A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918209 | ||||||
chr6:143918257
|
C | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+15105C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918257 | ||||||
chr6:143918333
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.598+15181A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918333 | ||||||
chr6:143918428
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0142 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.598+15276C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918428 | ||||||
chr6:143918512
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0116others(20): Show | 23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.598+15360G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918512 | ||||||
chr6:143918645
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.598+15493C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918645 | ||||||
chr6:143918844
|
A | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+15692A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918844 | ||||||
chr6:143918921
|
C | G | 16 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0108others(13): Show | 16 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+15769C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918921 | ||||||
chr6:143918939
|
G | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(111): Show | 115 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.598+15787G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918939 | ||||||
chr6:143918946
|
G | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(84): Show | 89 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.598+15794G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918946 | ||||||
chr6:143918958
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0240a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+15806G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918958 | ||||||
chr6:143919215
|
CTCTG | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00438.hp2 HG00738.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+16065_598+1606 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | |||||
chr6:143919215
|
CTCTGTG | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0054a0001c0001t0001g0058others(10): Show | 13 | HG01123.hp1 HG01168.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | |||||
chr6:143919215
|
CTCTGTGT others(1): Show |
C | 45 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0050others(42): Show | 47 | HG00408.hp2 HG00423.hp1 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | |||||
chr6:143919215
|
CTCTGTGT others(3): Show |
C | 6 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0074others(3): Show | 6 | NA18940.hp2 NA18949.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(14): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | |||||
chr6:143919215
|
CTCTGTGT others(5): Show |
C | 5 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0097others(2): Show | 5 | NA18959.hp1 NA18979.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | |||||
chr6:143919217
|
C | CTCTG | 3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 3 | HG02486.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.598+16066_598+1606 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
C | CTG | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0092others(35): Show | 38 | HG00673.hp1 HG01099.hp1 HG02027.hp2 others(35): Show |
intron_variant | MODIFIER | c.598+16113_598+1611 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
C | CTGTG | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0124others(10): Show | 13 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+16111_598+1611 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
C | CTGTGTG | 7 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0115others(4): Show | 7 | HG02572.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+16109_598+1611 others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0240a0001c0001t0001g0303a0001c0001t0001g0305others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+16107_598+1611 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.598+16103_598+1611 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
C | CTGTGTGT others(9): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0284 | 2 | HG00558.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.598+16099_598+1611 others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTG | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0107others(27): Show | 31 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.598+16113_598+1611 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTGTG | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0026others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(68): Show |
intron_variant | MODIFIER | c.598+16111_598+1611 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTGTGTG | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0128others(4): Show | 7 | HG00639.hp2 HG00673.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.598+16109_598+1611 others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTGTGTGT others(1): Show |
C | 8 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(5): Show | 8 | HG00733.hp2 HG02055.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+16107_598+1611 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+16105_598+1611 others(14): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTGTGTGT others(5): Show |
C | 2 | a0003c0003t0001g0034a0003c0003t0001g0035 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+16103_598+1611 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919217
|
CTGTGTGT others(17): Show |
C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01884.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.598+16091_598+1611 others(28): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | |||||
chr6:143919263
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0135a0001c0001t0001g0267 | 3 | HG03490.hp1 HG03710.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.598+16111G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919263 | ||||||
chr6:143919347
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.598+16195C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919347 | ||||||
chr6:143919389
|
G | GT | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 75 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.598+16243dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919389 | |||||
chr6:143919620
|
T | C | 8 | a0001c0001t0001g0188a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+16468T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919620 | ||||||
chr6:143919645
|
T | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00673.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.598+16493T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919645 | ||||||
chr6:143919691
|
T | G | 1 | a0001c0001t0001g0282 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.598+16539T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919691 | ||||||
chr6:143919762
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.598+16610G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919762 | ||||||
chr6:143919824
|
C | T | 8 | a0001c0001t0001g0188a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+16672C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919824 | ||||||
chr6:143919856
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+16704T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919856 | ||||||
chr6:143919866
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+16714G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919866 | ||||||
chr6:143919941
|
A | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+16789A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919941 | ||||||
chr6:143919985
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+16833T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919985 | ||||||
chr6:143920001
|
G | GA | 14 | a0001c0001t0001g0030a0001c0001t0001g0130a0001c0001t0001g0132others(11): Show | 14 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(11): Show |
intron_variant | MODIFIER | c.598+16858dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920001 | |||||
chr6:143920318
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0116 | 2 | HG01258.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598+17166T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920318 | ||||||
chr6:143920420
|
C | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-17229C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920420 | ||||||
chr6:143920509
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-17140A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920509 | ||||||
chr6:143920638
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.599-17011T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920638 | ||||||
chr6:143920684
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-16965G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920684 | ||||||
chr6:143920733
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.599-16916C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920733 | ||||||
chr6:143920736
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.599-16913C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920736 | ||||||
chr6:143920762
|
G | T | 9 | a0001c0001t0001g0281a0001c0001t0001g0296a0001c0001t0001g0297others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-16887G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920762 | ||||||
chr6:143920849
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0240a0004c0004t0001g0057 | 3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-16800A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920849 | ||||||
chr6:143920906
|
C | CA | 6 | a0001c0001t0001g0013a0001c0001t0001g0170a0001c0001t0001g0210others(3): Show | 6 | HG01934.hp2 HG02109.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-16725dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920906 | |||||
chr6:143920906
|
CA | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(125): Show | 130 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.599-16725delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920906 | |||||
chr6:143920906
|
CAA | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0044others(6): Show | 9 | HG02055.hp1 HG02300.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.599-16726_599-1672 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920906 | |||||
chr6:143921085
|
C | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-16564C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921085 | ||||||
chr6:143921213
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-16436T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921213 | ||||||
chr6:143921392
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.599-16257T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921392 | ||||||
chr6:143921541
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-16108C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921541 | ||||||
chr6:143921871
|
A | C | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.599-15778A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921871 | ||||||
chr6:143922148
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0313 | 2 | HG01099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.599-15501G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922148 | ||||||
chr6:143922176
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-15473A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922176 | ||||||
chr6:143922199
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.599-15450A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922199 | ||||||
chr6:143922372
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0308a0001c0001t0001g0317others(1): Show | 4 | HG02257.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-15277G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922372 | ||||||
chr6:143922442
|
G | A | 6 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0208others(3): Show | 6 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-15207G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922442 | ||||||
chr6:143923079
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 247 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.599-14570G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923079 | ||||||
chr6:143923154
|
C | A | 8 | a0001c0001t0001g0188a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-14495C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923154 | ||||||
chr6:143923736
|
T | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-13913T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923736 | ||||||
chr6:143923807
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.599-13842G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923807 | ||||||
chr6:143923968
|
T | C | 8 | a0001c0001t0001g0281a0001c0001t0001g0296a0001c0001t0001g0297others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-13681T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923968 | ||||||
chr6:143924089
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-13560C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924089 | ||||||
chr6:143924153
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.599-13496G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924153 | ||||||
chr6:143924276
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-13373A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924276 | ||||||
chr6:143924296
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-13353A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924296 | ||||||
chr6:143924349
|
T | TTA | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0047others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-13286_599-1328 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143924349 | |||||
chr6:143924474
|
A | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-13175A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924474 | ||||||
chr6:143924679
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-12970G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924679 | ||||||
chr6:143924760
|
GA | G | 7 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0196others(4): Show | 7 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-12886delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143924760 | |||||
chr6:143924769
|
A | G | 27 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(24): Show | 27 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.599-12880A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924769 | ||||||
chr6:143924977
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-12672G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924977 | ||||||
chr6:143925165
|
C | CT | 49 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0061others(46): Show | 49 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.599-12456dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925165
|
C | CTT | 21 | a0001c0001t0001g0078a0001c0001t0001g0106a0001c0001t0001g0116others(18): Show | 21 | HG00558.hp1 HG01258.hp1 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.599-12457_599-1245 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925165
|
C | CTTT | 7 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0131others(4): Show | 7 | HG01978.hp1 HG02257.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-12458_599-1245 others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925165
|
CT | C | 27 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0044others(24): Show | 27 | HG00733.hp1 HG01109.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.599-12456delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925165
|
CTT | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(16): Show | 19 | HG00140.hp2 HG00639.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.599-12457_599-1245 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925165
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0189 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.599-12468_599-1245 others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925165
|
CTTTTTTT others(7): Show |
C | 73 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 74 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.599-12469_599-1245 others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | |||||
chr6:143925171
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-12478T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925171 | ||||||
chr6:143925214
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0308a0001c0001t0001g0317others(1): Show | 4 | HG02257.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-12435C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925214 | ||||||
chr6:143925224
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-12425G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925224 | ||||||
chr6:143925237
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-12412G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925237 | ||||||
chr6:143925265
|
TC | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12381delC | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925265 | |||||
chr6:143925289
|
C | A | 1 | a0002c0002t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.599-12360C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925289 | ||||||
chr6:143925290
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.599-12359G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925290 | ||||||
chr6:143925290
|
G | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12359G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925290 | ||||||
chr6:143925300
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-12349C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925300 | ||||||
chr6:143925301
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105others(1): Show | 4 | HG02074.hp2 HG03540.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-12348G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925301 | ||||||
chr6:143925304
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12345C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925304 | ||||||
chr6:143925313
|
G | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12336G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925313 | ||||||
chr6:143925316
|
T | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12333T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925316 | ||||||
chr6:143925321
|
A | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0105 | 3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12328A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925321 | ||||||
chr6:143925410
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-12239C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925410 | ||||||
chr6:143925418
|
G | A | 27 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0116others(24): Show | 27 | HG00438.hp1 HG00558.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.599-12231G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925418 | ||||||
chr6:143925527
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.599-12122T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925527 | ||||||
chr6:143925536
|
C | CTT | 11 | a0001c0001t0001g0048a0001c0001t0001g0280a0002c0002t0001g0015others(8): Show | 11 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-12097_599-1209 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925536 | |||||
chr6:143925536
|
CT | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 223 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.599-12096delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925536 | |||||
chr6:143925542
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.599-12107T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925542 | ||||||
chr6:143925558
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.599-12091C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925558 | ||||||
chr6:143925578
|
C | G | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.599-12071C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925578 | ||||||
chr6:143925591
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.599-12058T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925591 | ||||||
chr6:143925605
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 75 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.599-12044C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925605 | ||||||
chr6:143926082
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.599-11567A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926082 | ||||||
chr6:143926249
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.599-11400C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926249 | ||||||
chr6:143926250
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.599-11399G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926250 | ||||||
chr6:143926250
|
G | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0047 | 3 | HG03098.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.599-11399G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926250 | ||||||
chr6:143926283
|
T | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(73): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.599-11366T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926283 | ||||||
chr6:143926366
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0038others(4): Show | 8 | HG01106.hp1 HG01358.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-11283C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926366 | ||||||
chr6:143926390
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-11259T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926390 | ||||||
chr6:143926408
|
T | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0170others(2): Show | 5 | HG01433.hp2 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-11241T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926408 | ||||||
chr6:143926413
|
G | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-11236G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926413 | ||||||
chr6:143926431
|
CTGT | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(70): Show | 75 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.599-11213_599-1121 others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926431 | |||||
chr6:143926493
|
A | AT | 126 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(123): Show | 127 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.599-11146dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926493 | |||||
chr6:143926533
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-11116A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926533 | ||||||
chr6:143926577
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-11072T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926577 | ||||||
chr6:143926624
|
T | G | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-11025T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926624 | ||||||
chr6:143926627
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.599-11022G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926627 | ||||||
chr6:143926695
|
A | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-10954A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926695 | ||||||
chr6:143926774
|
ATATATAA others(1): Show |
A | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-10873_599-1086 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926774 | |||||
chr6:143926779
|
T | G | 4 | a0001c0001t0001g0320a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-10870T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926779 | ||||||
chr6:143926828
|
C | CT | 33 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(30): Show | 34 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.599-10795dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926828 | |||||
chr6:143926828
|
CT | C | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0044others(24): Show | 27 | HG01192.hp1 HG01952.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.599-10795delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926828 | |||||
chr6:143926828
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-10806_599-1079 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926828 | |||||
chr6:143926860
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.599-10789G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926860 | ||||||
chr6:143926885
|
G | A | 1 | a0002c0002t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.599-10764G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926885 | ||||||
chr6:143926898
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-10751C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926898 | ||||||
chr6:143926920
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-10729C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926920 | ||||||
chr6:143926936
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.599-10713G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926936 | ||||||
chr6:143926953
|
G | GGCGCCCG others(5): Show |
146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 147 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.599-10689_599-1068 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926953 | |||||
chr6:143926955
|
C | CGCCCGCC others(5): Show |
1 | a0001c0001t0001g0268 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.599-10689_599-1068 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926955 | |||||
chr6:143927007
|
C | A | 147 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 148 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.599-10642C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927007 | ||||||
chr6:143927078
|
G | A | 3 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.599-10571G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927078 | ||||||
chr6:143927094
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-10555G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927094 | ||||||
chr6:143927111
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.599-10538C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927111 | ||||||
chr6:143927117
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.599-10532G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927117 | ||||||
chr6:143927216
|
T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0244a0001c0001t0001g0318 | 3 | HG00642.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.599-10433T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927216 | ||||||
chr6:143927332
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0236 | 3 | NA18983.hp2 NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.599-10317C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927332 | ||||||
chr6:143927472
|
G | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.599-10177G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927472 | ||||||
chr6:143927512
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.599-10137A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927512 | ||||||
chr6:143927565
|
T | G | 7 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0196others(4): Show | 7 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-10084T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927565 | ||||||
chr6:143927835
|
A | G | 4 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0131others(1): Show | 4 | HG00558.hp1 HG02129.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-9814A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927835 | ||||||
chr6:143928084
|
TTGTC | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0193 | 3 | NA18963.hp1 NA18984.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.599-9559_599-9556d others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928084 | |||||
chr6:143928252
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.599-9397C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928252 | ||||||
chr6:143928345
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-9304C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928345 | ||||||
chr6:143928347
|
A | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(22): Show | 25 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.599-9302A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928347 | ||||||
chr6:143928405
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(136): Show | 140 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.599-9244G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928405 | ||||||
chr6:143928460
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-9189T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928460 | ||||||
chr6:143928548
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.599-9101G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928548 | ||||||
chr6:143928565
|
G | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0078others(2): Show | 5 | NA18959.hp1 NA18979.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-9084G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928565 | ||||||
chr6:143928595
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.599-9054G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928595 | ||||||
chr6:143928795
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-8854A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928795 | ||||||
chr6:143928824
|
G | GT | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0026others(19): Show | 22 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.599-8814dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928824 | |||||
chr6:143928824
|
G | GTT | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 229 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.599-8815_599-8814d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928824 | |||||
chr6:143928824
|
G | GTTT | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0049others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-8816_599-8814d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928824 | |||||
chr6:143929069
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.599-8580G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929069 | ||||||
chr6:143929078
|
T | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0001t0001g0325 | 4 | HG00408.hp2 NA18971.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-8571T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929078 | ||||||
chr6:143929200
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-8449C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929200 | ||||||
chr6:143929231
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-8418A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929231 | ||||||
chr6:143929283
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.599-8366C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929283 | ||||||
chr6:143929330
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.599-8319T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929330 | ||||||
chr6:143929374
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.599-8275G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929374 | ||||||
chr6:143929375
|
A | T | 1 | a0001c0001t0001g0319 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.599-8274A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929375 | ||||||
chr6:143929465
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.599-8184G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929465 | ||||||
chr6:143929498
|
A | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.599-8151A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929498 | ||||||
chr6:143929509
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.599-8140A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929509 | ||||||
chr6:143929516
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.599-8133T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929516 | ||||||
chr6:143929571
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.599-8078T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929571 | ||||||
chr6:143929604
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.599-8045G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929604 | ||||||
chr6:143929682
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-7967G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929682 | ||||||
chr6:143929683
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.599-7966A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929683 | ||||||
chr6:143929705
|
TTTGTTG | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-7929_599-7924d others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143929705 | |||||
chr6:143929892
|
T | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 234 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.599-7757T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929892 | ||||||
chr6:143929995
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.599-7654G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929995 | ||||||
chr6:143930224
|
C | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(157): Show | 161 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.599-7425C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930224 | ||||||
chr6:143930237
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.599-7412T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930237 | ||||||
chr6:143930367
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-7282A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930367 | ||||||
chr6:143930381
|
CT | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 167 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.599-7248delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143930381 | |||||
chr6:143930381
|
CTT | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(76): Show | 80 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.599-7249_599-7248d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143930381 | |||||
chr6:143930385
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.599-7264T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930385 | ||||||
chr6:143930386
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-7263T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930386 | ||||||
chr6:143930426
|
G | A | 9 | a0001c0001t0001g0281a0001c0001t0001g0296a0001c0001t0001g0297others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-7223G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930426 | ||||||
chr6:143930449
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.599-7200C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930449 | ||||||
chr6:143930450
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.599-7199G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930450 | ||||||
chr6:143930473
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.599-7176G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930473 | ||||||
chr6:143930545
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(136): Show | 140 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.599-7104G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930545 | ||||||
chr6:143930549
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.599-7100G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930549 | ||||||
chr6:143930591
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 256 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.599-7058G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930591 | ||||||
chr6:143930651
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.599-6998A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930651 | ||||||
chr6:143930882
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-6767A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930882 | ||||||
chr6:143931221
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0203 | 2 | HG00408.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.599-6428A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931221 | ||||||
chr6:143931239
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-6410C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931239 | ||||||
chr6:143931255
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.599-6394A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931255 | ||||||
chr6:143931280
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-6369T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931280 | ||||||
chr6:143931365
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-6284C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931365 | ||||||
chr6:143931404
|
A | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-6245A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931404 | ||||||
chr6:143931462
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.599-6187G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931462 | ||||||
chr6:143931506
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-6143T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931506 | ||||||
chr6:143931603
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-6046C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931603 | ||||||
chr6:143931709
|
T | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 231 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.599-5940T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931709 | ||||||
chr6:143931756
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.599-5893A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931756 | ||||||
chr6:143931811
|
A | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-5838A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931811 | ||||||
chr6:143931844
|
T | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(139): Show | 143 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.599-5805T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931844 | ||||||
chr6:143931848
|
ACTT | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0102others(3): Show | 6 | HG03017.hp2 HG03579.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-5785_599-5783d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143931848 | |||||
chr6:143931862
|
TTC | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 212 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.599-5785_599-5784d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143931862 | |||||
chr6:143931863
|
TC | T | 25 | a0001c0001t0001g0048a0001c0001t0001g0065a0001c0001t0001g0130others(22): Show | 25 | HG02109.hp1 HG02451.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.599-5785delC | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931863 | ||||||
chr6:143931864
|
CTT | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0128others(8): Show | 11 | HG01192.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-5768_599-5767d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143931864 | |||||
chr6:143931884
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0317 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-5765A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931884 | ||||||
chr6:143931903
|
G | A | 1 | a0002c0002t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.599-5746G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931903 | ||||||
chr6:143931943
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-5706C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931943 | ||||||
chr6:143931958
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(139): Show | 143 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.599-5691A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931958 | ||||||
chr6:143931967
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.599-5682C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931967 | ||||||
chr6:143932094
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-5555C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932094 | ||||||
chr6:143932095
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.599-5554G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932095 | ||||||
chr6:143932211
|
T | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(139): Show | 143 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.599-5438T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932211 | ||||||
chr6:143932250
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.599-5399T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932250 | ||||||
chr6:143932447
|
G | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(139): Show | 143 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.599-5202G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932447 | ||||||
chr6:143932636
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-5013C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932636 | ||||||
chr6:143932823
|
T | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(72): Show | 77 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.599-4826T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932823 | ||||||
chr6:143932824
|
G | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-4825G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932824 | ||||||
chr6:143932844
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-4805C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932844 | ||||||
chr6:143932884
|
G | A | 8 | a0001c0001t0001g0188a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-4765G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932884 | ||||||
chr6:143932976
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-4673G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932976 | ||||||
chr6:143933143
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.599-4506A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933143 | ||||||
chr6:143933156
|
C | T | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(138): Show | 142 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.599-4493C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933156 | ||||||
chr6:143933459
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01081.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.599-4190T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933459 | ||||||
chr6:143933607
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.599-4042C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933607 | ||||||
chr6:143933608
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0303others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-4041G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933608 | ||||||
chr6:143933674
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-3975G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933674 | ||||||
chr6:143933808
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-3841C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933808 | ||||||
chr6:143933858
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(82): Show | 87 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.599-3791C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933858 | ||||||
chr6:143933910
|
T | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(111): Show | 115 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.599-3739T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933910 | ||||||
chr6:143933965
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-3684G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933965 | ||||||
chr6:143933980
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-3669A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933980 | ||||||
chr6:143934074
|
C | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-3575C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934074 | ||||||
chr6:143934115
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 231 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.599-3534G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934115 | ||||||
chr6:143934255
|
G | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.599-3394G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934255 | ||||||
chr6:143934329
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.599-3320G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934329 | ||||||
chr6:143934358
|
T | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 231 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.599-3291T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934358 | ||||||
chr6:143934375
|
T | A | 1 | a0001c0001t0001g0261 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.599-3274T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934375 | ||||||
chr6:143934597
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG00733.hp1 HG02602.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-3052A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934597 | ||||||
chr6:143934683
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.599-2966C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934683 | ||||||
chr6:143934756
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599-2893G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934756 | ||||||
chr6:143935088
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 235 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.599-2561C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935088 | ||||||
chr6:143935122
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0116others(20): Show | 23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.599-2527C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935122 | ||||||
chr6:143935140
|
T | TGGTGGGC others(2): Show |
232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 235 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.599-2503_599-2502i others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935140 | |||||
chr6:143935255
|
T | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-2394T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935255 | ||||||
chr6:143935326
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-2323A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935326 | ||||||
chr6:143935400
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(76): Show | 81 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.599-2249C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935400 | ||||||
chr6:143935431
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-2218G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935431 | ||||||
chr6:143935446
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-2203C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935446 | ||||||
chr6:143935581
|
T | G | 1 | a0001c0001t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.599-2068T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935581 | ||||||
chr6:143935616
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.599-2033A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935616 | ||||||
chr6:143935619
|
C | A | 20 | a0001c0001t0001g0048a0001c0001t0001g0130a0001c0001t0001g0132others(17): Show | 20 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.599-2030C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935619 | ||||||
chr6:143935625
|
T | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0139others(4): Show | 7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-2024T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935625 | ||||||
chr6:143935628
|
A | G | 8 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0079others(5): Show | 8 | HG01943.hp1 HG01952.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-2021A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935628 | ||||||
chr6:143935646
|
C | CT | 29 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0040others(26): Show | 29 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.599-1975dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
C | CTT | 11 | a0001c0001t0001g0056a0001c0001t0001g0112a0001c0001t0001g0114others(8): Show | 11 | HG01099.hp1 HG02040.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1976_599-1975d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
C | CTTT | 61 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(58): Show | 62 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.599-1977_599-1975d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
C | CTTTT | 11 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0092others(8): Show | 11 | HG01109.hp1 HG01433.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1978_599-1975d others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
C | CTTTTT | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0116others(16): Show | 19 | HG01081.hp2 HG01258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.599-1979_599-1975d others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
C | CTTTTTT | 10 | a0001c0001t0001g0111a0001c0001t0001g0120a0001c0001t0001g0121others(7): Show | 10 | HG01978.hp1 HG02129.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.599-1980_599-1975d others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
C | CTTTTTTT | 6 | a0001c0001t0001g0013a0001c0001t0001g0129a0001c0001t0001g0131others(3): Show | 6 | NA18940.hp1 NA18963.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-1981_599-1975d others(9): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
CT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0036others(5): Show | 8 | HG00558.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-1975delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
CTT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0046others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-1976_599-1975d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
CTTT | C | 6 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0143others(3): Show | 6 | NA19011.hp2 NA19056.hp1 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-1977_599-1975d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
CTTTTT | C | 11 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(8): Show | 11 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1979_599-1975d others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-1985_599-1975d others(13): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935646
|
CTTTTTTT others(7): Show |
C | 13 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(10): Show | 13 | HG02080.hp2 HG02135.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-1988_599-1975d others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | |||||
chr6:143935674
|
T | G | 20 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0059others(17): Show | 20 | HG02080.hp2 HG02135.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.599-1975T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935674 | ||||||
chr6:143935674
|
T | TTG | 42 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(39): Show | 44 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.599-1975_599-1974i others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935674 | ||||||
chr6:143935674
|
T | TTTG | 20 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0074others(17): Show | 20 | HG01358.hp1 HG01943.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-1975_599-1974i others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935674 | ||||||
chr6:143935687
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-1962C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935687 | ||||||
chr6:143935728
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-1921C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935728 | ||||||
chr6:143935777
|
C | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.599-1872C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935777 | ||||||
chr6:143935884
|
A | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-1765A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935884 | ||||||
chr6:143935960
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 235 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.599-1689G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935960 | ||||||
chr6:143935992
|
A | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 235 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.599-1657A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935992 | ||||||
chr6:143936105
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | NA18950.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.599-1544A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936105 | ||||||
chr6:143936133
|
C | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 237 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.599-1516C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936133 | ||||||
chr6:143936202
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.599-1447A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936202 | ||||||
chr6:143936227
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.599-1422T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936227 | ||||||
chr6:143936307
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(112): Show | 116 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.599-1342G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936307 | ||||||
chr6:143936315
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.599-1334A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936315 | ||||||
chr6:143936415
|
A | T | 1 | a0001c0001t0001g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-1234A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936415 | ||||||
chr6:143936502
|
A | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0111a0001c0001t0001g0116others(20): Show | 23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.599-1147A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936502 | ||||||
chr6:143937107
|
T | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(140): Show | 144 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.599-542T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937107 | ||||||
chr6:143937216
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-433T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937216 | ||||||
chr6:143937222
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.599-427T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937222 | ||||||
chr6:143937249
|
G | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0280a0001c0001t0001g0283others(9): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-400G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937249 | ||||||
chr6:143937314
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-335G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937314 | ||||||
chr6:143937445
|
G | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(135): Show | 139 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.599-204G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937445 | ||||||
chr6:143937482
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 237 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.599-167G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937482 | ||||||
chr6:143937513
|
C | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.599-136C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937513 | ||||||
chr6:143937533
|
C | CA | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.599-108dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143937533 | |||||
chr6:143937585
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-64A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937585 | ||||||
chr6:143937639
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.599-10G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937639 | ||||||
chr6:143937744
|
A | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0088others(4): Show | 7 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.*14+11A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937744 | ||||||
chr6:143937753
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0240 | 2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.*14+20G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937753 | ||||||
chr6:143937761
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.*14+28A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937761 | ||||||
chr6:143937793
|
G | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.*14+60G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937793 | ||||||
chr6:143937882
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*14+149T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937882 |