geneid | 892 |
---|---|
ensemblid | ENSG00000112237.13 |
hgncid | 1581 |
symbol | CCNC |
name | cyclin C |
refseq_nuc | NM_005190.4 |
refseq_prot | NP_005181.2 |
ensembl_nuc | ENST00000520429.6 |
ensembl_prot | ENSP00000428982.1 |
mane_status | MANE Select |
chr | chr6 |
start | 99542387 |
end | 99568660 |
strand | - |
ver | v1.2 |
region | chr6:99542387-99568660 |
region5000 | chr6:99537387-99573660 |
regionname0 | CCNC_chr6_99542387_99568660 |
regionname5000 | CCNC_chr6_99537387_99573660 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 283 | 410 | 84 | 78 | 184 | 14 | 48 | 154 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1302 | 331 | 76 | 61 | 150 | 11 | 31 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0002 | 0/0 | 1302 | 68 | 5 | 13 | 32 | 3 | 15 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0003 | 0/0 | 1302 | 4 | 0 | 3 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0004 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0005 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0006 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0007 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0008 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0009 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
t0010 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 40 | 0 | 2 | 35 | 0 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0002 | 1/0 | 14 | 1 | 12 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0003 | 0/0 | 13 | 2 | 1 | 10 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0004 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0005 | 0/0 | 12 | 1 | 4 | 2 | 1 | 4 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0007 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0009 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0010 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0011 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0012 | 0/0 | 6 | 4 | 1 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0013 | 0/1 | 6 | 0 | 1 | 0 | 1 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0015 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0020 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0021 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0024 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 852 | 408 | 84 | 78 | 182 | 14 | 48 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0002 | 0/0 | 852 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2153 | 329 | 76 | 61 | 148 | 11 | 31 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0002 | 0/0 | 2153 | 68 | 5 | 13 | 32 | 3 | 15 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0003 | 0/0 | 2153 | 4 | 0 | 3 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0004 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0005 | 0/0 | 2153 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0006 | 0/0 | 2153 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0007 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0008 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0009 | 0/0 | 2153 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0001t0010 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
a0001c0002t0001 | 0/0 | 2153 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | copy fasta | chr6 | 99537387 | 99573660 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 40 | 0 | 2 | 35 | 0 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0002 | 1/0 | 14 | 1 | 12 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0003 | 0/0 | 13 | 2 | 1 | 10 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0004 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0010 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0011 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0012 | 0/0 | 6 | 4 | 1 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0013 | 0/1 | 6 | 0 | 1 | 0 | 1 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0005 | 0/0 | 12 | 1 | 4 | 2 | 1 | 4 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0009 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0021 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0187 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0103 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0153 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0137 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0088 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ASW | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0209 | SAS | GIH | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0013 | REF | REF | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99562882
|
T | C | 1 | a0001c0002 | 2 | NA18949.hp1 NA19012.hp1 |
synonymous_variant | LOW | c.99A>G | p.Ser33Ser | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/12 | 232/2153 | 99/852 | 33/283 | chr6 | 99562882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99542488
|
T | C | 1 | a0001c0001t0007 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 1067 | chr6 | 99542488 | |||||
chr6:99542576
|
C | T | 1 | a0001c0001t0006 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 979 | chr6 | 99542576 | |||||
chr6:99542809
|
G | A | 1 | a0001c0001t0002 | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 746 | chr6 | 99542809 | |||||
chr6:99542976
|
T | C | 1 | a0001c0001t0008 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*579A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 579 | chr6 | 99542976 | |||||
chr6:99542980
|
T | C | 1 | a0001c0001t0002 | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*575A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 575 | chr6 | 99542980 | |||||
chr6:99543046
|
C | T | 1 | a0001c0001t0005 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 509 | chr6 | 99543046 | |||||
chr6:99543210
|
A | G | 1 | a0001c0001t0004 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*345T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 345 | chr6 | 99543210 | |||||
chr6:99543317
|
T | C | 1 | a0001c0001t0009 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*238A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 238 | chr6 | 99543317 | |||||
chr6:99543416
|
T | C | 1 | a0001c0001t0010 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 139 | chr6 | 99543416 | |||||
chr6:99568541
|
C | G | 1 | a0001c0001t0003 | 4 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/12 | 14 | chr6 | 99568541 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99543620
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0170 | 2 | NA18957.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.798-11C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99543620 | ||||||
chr6:99543702
|
G | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0050others(3): Show | 8 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-93C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99543702 | ||||||
chr6:99543834
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.798-225A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99543834 | ||||||
chr6:99544014
|
CAA | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0087others(25): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.798-407_798-406del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544014 | ||||||
chr6:99544014
|
CAAA | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 335 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.798-408_798-406del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544014 | ||||||
chr6:99544089
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.798-480C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544089 | ||||||
chr6:99544116
|
GAAAATGC others(15): Show |
G | 1 | a0001c0001t0001g0036 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.798-529_798-508del others(22): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544116 | ||||||
chr6:99544630
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.797+482A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544630 | ||||||
chr6:99544729
|
G | A | 1 | a0001c0001t0001g0015 | 5 | HG00323.hp2 HG00733.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.797+383C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544729 | ||||||
chr6:99544745
|
G | GA | 25 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0026others(22): Show | 44 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.797+366dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544745 | ||||||
chr6:99544745
|
G | GAA | 7 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0087others(4): Show | 14 | HG00423.hp1 HG00544.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.797+365_797+366dup others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544745 | ||||||
chr6:99544745
|
GA | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(136): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.797+366delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544745 | ||||||
chr6:99544751
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.797+361T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544751 | ||||||
chr6:99544854
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.797+258T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544854 | ||||||
chr6:99545312
|
C | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.679-82G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545312 | ||||||
chr6:99545350
|
G | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0036others(3): Show | 14 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.679-120C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545350 | ||||||
chr6:99545392
|
G | A | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.679-162C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545392 | ||||||
chr6:99545665
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.679-435C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545665 | ||||||
chr6:99545779
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.679-549G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545779 | ||||||
chr6:99545828
|
AG | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0166 | 4 | NA18940.hp1 NA18955.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+566delC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545828 | ||||||
chr6:99545866
|
G | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.678+529C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545866 | ||||||
chr6:99545992
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.678+403C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545992 | ||||||
chr6:99546032
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.678+363C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546032 | ||||||
chr6:99546113
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.678+282T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546113 | ||||||
chr6:99546172
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.678+223C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546172 | ||||||
chr6:99546186
|
G | A | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.678+209C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546186 | ||||||
chr6:99546380
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.678+15G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546380 | ||||||
chr6:99546630
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-156T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546630 | ||||||
chr6:99546722
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0174a0001c0001t0001g0175 | 5 | HG01891.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-248T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546722 | ||||||
chr6:99546888
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.599-414C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546888 | ||||||
chr6:99546953
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.599-479G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546953 | ||||||
chr6:99547060
|
T | TACA | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.599-587_599-586ins others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547060 | ||||||
chr6:99547088
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.599-614T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547088 | ||||||
chr6:99547177
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.599-703G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547177 | ||||||
chr6:99547444
|
G | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.599-970C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547444 | ||||||
chr6:99547468
|
T | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0102others(5): Show | 10 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.599-994A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547468 | ||||||
chr6:99547486
|
C | CA | 42 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(39): Show | 95 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.599-1013dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547486 | ||||||
chr6:99547600
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-1126T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547600 | ||||||
chr6:99547647
|
T | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.599-1173A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547647 | ||||||
chr6:99547650
|
C | G | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0065others(19): Show | 24 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.599-1176G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547650 | ||||||
chr6:99547753
|
A | G | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.599-1279T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547753 | ||||||
chr6:99548099
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.598+1409C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548099 | ||||||
chr6:99548101
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.598+1407C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548101 | ||||||
chr6:99548180
|
C | T | 4 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0053others(1): Show | 6 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+1328G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548180 | ||||||
chr6:99548486
|
AAG | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0029others(20): Show | 40 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.598+1020_598+1021d others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548486 | ||||||
chr6:99548540
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.598+968A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548540 | ||||||
chr6:99548576
|
AG | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.598+931delC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548576 | ||||||
chr6:99548751
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.598+757G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548751 | ||||||
chr6:99548772
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.598+736G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548772 | ||||||
chr6:99548773
|
A | AG | 3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0147 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+734dupC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548773 | ||||||
chr6:99548802
|
CAA | C | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0065others(24): Show | 29 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.598+704_598+705del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548802 | ||||||
chr6:99548802
|
CAAA | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(124): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.598+703_598+705del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548802 | ||||||
chr6:99548802
|
CAAAA | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(52): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.598+702_598+705del others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548802 | ||||||
chr6:99548918
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.598+590G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548918 | ||||||
chr6:99548949
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.598+559A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548949 | ||||||
chr6:99549076
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598+432A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549076 | ||||||
chr6:99549081
|
GTAC | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0203 | 3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.598+424_598+426del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549081 | ||||||
chr6:99549172
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.598+336C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549172 | ||||||
chr6:99549288
|
CA | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(89): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.598+219delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549288 | ||||||
chr6:99549288
|
CAA | C | 54 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(51): Show | 89 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.598+218_598+219del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549288 | ||||||
chr6:99549289
|
A | T | 3 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0056 | 4 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+219T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549289 | ||||||
chr6:99549290
|
A | C | 3 | a0001c0001t0002g0031a0001c0001t0002g0053a0001c0001t0002g0056 | 4 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+218T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549290 | ||||||
chr6:99549445
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.598+63A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549445 | ||||||
chr6:99549951
|
TCA | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.530+265_530+266del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99549951 | ||||||
chr6:99549957
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.530+261A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99549957 | ||||||
chr6:99549977
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.530+241G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99549977 | ||||||
chr6:99550166
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.530+52T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99550166 | ||||||
chr6:99550641
|
C | A | 1 | a0001c0001t0001g0123 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.439-332G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550641 | ||||||
chr6:99550642
|
A | C | 1 | a0001c0001t0001g0123 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.439-333T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550642 | ||||||
chr6:99550659
|
A | ATAATCTA others(319): Show |
1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(326): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(321): Show |
1 | a0001c0001t0001g0034 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(328): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(327): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0079 | 2 | HG03225.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(334): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(328): Show |
1 | a0001c0001t0001g0078 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(335): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(329): Show |
1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(336): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(323): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0085 | 3 | HG00735.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(330): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(324): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG02886.hp2 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(331): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(325): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(332): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(326): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0204 | 3 | HG02723.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.438+333_438+334ins others(333): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(337): Show |
1 | a0001c0001t0001g0071 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(344): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(339): Show |
1 | a0001c0001t0004g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(346): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(340): Show |
1 | a0001c0001t0001g0077 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(347): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(333): Show |
1 | a0001c0001t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(340): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550659
|
A | ATAATCTA others(345): Show |
1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(352): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | ||||||
chr6:99550685
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.438+308G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550685 | ||||||
chr6:99550771
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.438+222A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550771 | ||||||
chr6:99550876
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.438+117G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550876 | ||||||
chr6:99550943
|
C | T | 1 | a0001c0001t0001g0017 | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+50G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550943 | ||||||
chr6:99550961
|
T | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0146 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.438+32A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550961 | ||||||
chr6:99551143
|
A | G | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.403-115T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551143 | ||||||
chr6:99551149
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.403-121A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551149 | ||||||
chr6:99551150
|
T | A | 4 | a0001c0001t0002g0023a0001c0001t0002g0032a0001c0001t0002g0047others(1): Show | 7 | HG00621.hp1 HG02132.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-122A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551150 | ||||||
chr6:99551439
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.402+401G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551439 | ||||||
chr6:99551679
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.402+161A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551679 | ||||||
chr6:99551717
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.402+123C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551717 | ||||||
chr6:99551735
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.402+105A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551735 | ||||||
chr6:99551906
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.347-11A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551906 | ||||||
chr6:99551907
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.347-12T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551907 | ||||||
chr6:99551917
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.347-22A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551917 | ||||||
chr6:99551966
|
A | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0212 | 3 | HG01070.hp2 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.347-71T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551966 | ||||||
chr6:99552003
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.347-108A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552003 | ||||||
chr6:99552109
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-214T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552109 | ||||||
chr6:99552258
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0147 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.347-363T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552258 | ||||||
chr6:99552609
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.347-714T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552609 | ||||||
chr6:99552922
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-1027C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552922 | ||||||
chr6:99552966
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-1071G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552966 | ||||||
chr6:99553014
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.347-1119A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553014 | ||||||
chr6:99553039
|
CA | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.347-1145delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553039 | ||||||
chr6:99553235
|
G | A | 1 | a0001c0001t0001g0042 | 2 | NA18940.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.347-1340C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553235 | ||||||
chr6:99553377
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.347-1482G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553377 | ||||||
chr6:99553430
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-1535G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553430 | ||||||
chr6:99553541
|
C | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0198 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.347-1646G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553541 | ||||||
chr6:99553565
|
A | G | 1 | a0001c0001t0002g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.347-1670T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553565 | ||||||
chr6:99553662
|
A | G | 1 | a0001c0001t0008g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.347-1767T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553662 | ||||||
chr6:99554097
|
T | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.347-2202A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554097 | ||||||
chr6:99554210
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-2315G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554210 | ||||||
chr6:99554211
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0203 | 3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.347-2316C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554211 | ||||||
chr6:99554510
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-2615T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554510 | ||||||
chr6:99554569
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.347-2674T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554569 | ||||||
chr6:99554617
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.347-2722T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554617 | ||||||
chr6:99554636
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.347-2741A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554636 | ||||||
chr6:99554742
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-2847G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554742 | ||||||
chr6:99554960
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.347-3065C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554960 | ||||||
chr6:99554991
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0008g0088 | 6 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-3096T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554991 | ||||||
chr6:99555027
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.347-3132A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555027 | ||||||
chr6:99555069
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-3174A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555069 | ||||||
chr6:99555386
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0083 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.346+3111A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555386 | ||||||
chr6:99555411
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0148a0001c0001t0001g0158others(2): Show | 7 | HG00639.hp1 HG01346.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+3086T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555411 | ||||||
chr6:99555431
|
G | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.346+3066C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555431 | ||||||
chr6:99555436
|
CT | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.346+3060delA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555436 | ||||||
chr6:99555450
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.346+3047A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555450 | ||||||
chr6:99555463
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+3034T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555463 | ||||||
chr6:99555518
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.346+2979C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555518 | ||||||
chr6:99555533
|
GC | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0147 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2963delG | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555533 | ||||||
chr6:99555536
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0147 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2961A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555536 | ||||||
chr6:99555537
|
A | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0147 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2960T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555537 | ||||||
chr6:99555570
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+2927G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555570 | ||||||
chr6:99555602
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.346+2895A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555602 | ||||||
chr6:99555649
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.346+2848G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555649 | ||||||
chr6:99555684
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0008g0088 | 5 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+2813G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555684 | ||||||
chr6:99555768
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+2729A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555768 | ||||||
chr6:99556004
|
GTTC | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.346+2490_346+2492d others(5): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556004 | ||||||
chr6:99556210
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.346+2287G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556210 | ||||||
chr6:99556296
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.346+2201A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556296 | ||||||
chr6:99556378
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.346+2119A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556378 | ||||||
chr6:99556554
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.346+1943G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556554 | ||||||
chr6:99556675
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.346+1822G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556675 | ||||||
chr6:99556685
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.346+1812G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556685 | ||||||
chr6:99556779
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+1718C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556779 | ||||||
chr6:99556812
|
C | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346+1685G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556812 | ||||||
chr6:99556812
|
C | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1685G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556812 | ||||||
chr6:99556819
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.346+1678C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556819 | ||||||
chr6:99556819
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346+1678C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556819 | ||||||
chr6:99556910
|
G | C | 1 | a0001c0001t0002g0056 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+1587C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556910 | ||||||
chr6:99556936
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.346+1561T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556936 | ||||||
chr6:99556956
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.346+1541C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556956 | ||||||
chr6:99557009
|
A | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0058 | 5 | HG02080.hp1 NA18943.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1488T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557009 | ||||||
chr6:99557049
|
ATCTAAC | A | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1442_346+1447d others(8): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557049 | ||||||
chr6:99557077
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.346+1420G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557077 | ||||||
chr6:99557112
|
T | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0138 | 2 | NA18991.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.346+1385A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557112 | ||||||
chr6:99557121
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.346+1376G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557121 | ||||||
chr6:99557284
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+1213T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557284 | ||||||
chr6:99557355
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0065others(19): Show | 24 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.346+1142A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557355 | ||||||
chr6:99557416
|
T | C | 1 | a0001c0001t0005g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.346+1081A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557416 | ||||||
chr6:99557421
|
G | A | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1076C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557421 | ||||||
chr6:99557438
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0019others(28): Show | 58 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.346+1059C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557438 | ||||||
chr6:99557503
|
G | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(61): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.346+994C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557503 | ||||||
chr6:99557503
|
G | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0205 | 2 | HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.346+994C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557503 | ||||||
chr6:99557561
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.346+936G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557561 | ||||||
chr6:99557776
|
G | A | 35 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(32): Show | 67 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.346+721C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557776 | ||||||
chr6:99557788
|
CA | C | 38 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0072others(35): Show | 69 | HG00099.hp1 HG00544.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.346+708delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557788 | ||||||
chr6:99557788
|
CAA | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG02257.hp2 HG02738.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+707_346+708del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557788 | ||||||
chr6:99557801
|
A | AG | 9 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0025others(6): Show | 20 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.346+695_346+696ins others(1): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557801 | ||||||
chr6:99557803
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.346+694T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557803 | ||||||
chr6:99557805
|
A | AAG | 12 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0042others(9): Show | 27 | HG00140.hp1 HG00609.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+691_346+692ins others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557805 | ||||||
chr6:99557805
|
A | AG | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(67): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.346+691_346+692ins others(1): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557805 | ||||||
chr6:99557805
|
A | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0025others(7): Show | 21 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.346+692T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557805 | ||||||
chr6:99557807
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(48): Show | 93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.346+690T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557807 | ||||||
chr6:99557809
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(48): Show | 93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.346+688C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557809 | ||||||
chr6:99557810
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.346+687T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557810 | ||||||
chr6:99557810
|
AAAG | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(74): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.346+684_346+686del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557810 | ||||||
chr6:99557811
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(48): Show | 93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.346+686T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557811 | ||||||
chr6:99557812
|
AG | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0042others(13): Show | 31 | HG00140.hp1 HG00609.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.346+684delC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557812 | ||||||
chr6:99557813
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(48): Show | 93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.346+684C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557813 | ||||||
chr6:99557813
|
G | GA | 8 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0089others(5): Show | 8 | HG02257.hp2 HG02738.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+683dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557813 | ||||||
chr6:99557868
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346+629A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557868 | ||||||
chr6:99557899
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.346+598C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557899 | ||||||
chr6:99557944
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.346+553G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557944 | ||||||
chr6:99557978
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.346+519T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557978 | ||||||
chr6:99557986
|
C | T | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0066others(18): Show | 23 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.346+511G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557986 | ||||||
chr6:99558052
|
C | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+445G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558052 | ||||||
chr6:99558094
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0042others(12): Show | 29 | HG00544.hp2 HG00609.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.346+403C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558094 | ||||||
chr6:99558108
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346+389G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558108 | ||||||
chr6:99558144
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.346+353T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558144 | ||||||
chr6:99558196
|
T | C | 2 | a0001c0001t0002g0016a0001c0001t0002g0058 | 5 | HG02080.hp1 NA18943.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+301A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558196 | ||||||
chr6:99558204
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.346+293C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558204 | ||||||
chr6:99558317
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.346+180T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558317 | ||||||
chr6:99558368
|
T | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.346+129A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558368 | ||||||
chr6:99558620
|
T | C | 1 | a0001c0001t0008g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295-72A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99558620 | ||||||
chr6:99558815
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0190 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.295-267C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99558815 | ||||||
chr6:99558861
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.295-313A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99558861 | ||||||
chr6:99559147
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.295-599A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559147 | ||||||
chr6:99559191
|
T | TA | 17 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0070others(14): Show | 20 | HG00323.hp1 HG00423.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.295-644dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559191 | ||||||
chr6:99559197
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.295-649T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559197 | ||||||
chr6:99559362
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0025others(6): Show | 20 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-814A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559362 | ||||||
chr6:99559402
|
T | TA | 3 | a0001c0001t0001g0038a0001c0001t0001g0131a0001c0001t0001g0132 | 4 | HG01175.hp2 HG01358.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-855dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559402 | ||||||
chr6:99559525
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295-977A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559525 | ||||||
chr6:99559652
|
TA | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(89): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.295-1105delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559652 | ||||||
chr6:99559662
|
AT | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.295-1115delA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559662 | ||||||
chr6:99559663
|
T | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 14 | HG01175.hp2 HG01261.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-1115A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559663 | ||||||
chr6:99559720
|
C | CT | 6 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0147others(3): Show | 6 | HG02738.hp1 HG04204.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-1173dupA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559720 | ||||||
chr6:99559720
|
CT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.295-1173delA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559720 | ||||||
chr6:99559843
|
C | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0174a0001c0001t0001g0175 | 5 | HG01891.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1295G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559843 | ||||||
chr6:99559880
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.295-1332G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559880 | ||||||
chr6:99559908
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.295-1360G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559908 | ||||||
chr6:99560025
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.294+1342T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560025 | ||||||
chr6:99560121
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.294+1246T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560121 | ||||||
chr6:99560213
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.294+1154G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560213 | ||||||
chr6:99560259
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.294+1108A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560259 | ||||||
chr6:99560368
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+999A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560368 | ||||||
chr6:99560395
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.294+972C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560395 | ||||||
chr6:99560411
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.294+956G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560411 | ||||||
chr6:99560530
|
CAACTCTA others(7): Show |
C | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.294+823_294+836del others(14): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560530 | ||||||
chr6:99560544
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.294+823C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560544 | ||||||
chr6:99560716
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0029others(19): Show | 39 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.294+651G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560716 | ||||||
chr6:99560759
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.294+608G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560759 | ||||||
chr6:99560952
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.294+415A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560952 | ||||||
chr6:99561024
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.294+343G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99561024 | ||||||
chr6:99561754
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.140-73G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561754 | ||||||
chr6:99561800
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.140-119T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561800 | ||||||
chr6:99561815
|
A | C | 1 | a0001c0001t0002g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.140-134T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561815 | ||||||
chr6:99561878
|
TAAACAAC others(4): Show |
T | 2 | a0001c0001t0001g0207a0001c0001t0002g0220 | 2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.140-208_140-198del others(11): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561878 | ||||||
chr6:99561974
|
C | G | 1 | a0001c0001t0002g0216 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.140-293G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561974 | ||||||
chr6:99562041
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.140-360A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562041 | ||||||
chr6:99562290
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.139+552C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562290 | ||||||
chr6:99562371
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.139+471G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562371 | ||||||
chr6:99562379
|
C | CA | 21 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0029others(18): Show | 38 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.139+462dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562379 | ||||||
chr6:99562507
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0203 | 3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.139+335G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562507 | ||||||
chr6:99562727
|
G | C | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.139+115C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562727 | ||||||
chr6:99562756
|
A | C | 1 | a0001c0001t0002g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139+86T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562756 | ||||||
chr6:99562777
|
AC | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.139+64delG | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562777 | ||||||
chr6:99563177
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.33-229A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563177 | ||||||
chr6:99563243
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(57): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.33-295G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563243 | ||||||
chr6:99563636
|
G | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.33-688C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563636 | ||||||
chr6:99563657
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.33-709A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563657 | ||||||
chr6:99563658
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.33-710G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563658 | ||||||
chr6:99563904
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.33-956T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563904 | ||||||
chr6:99564051
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.33-1103A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564051 | ||||||
chr6:99564052
|
G | C | 1 | a0001c0001t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.33-1104C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564052 | ||||||
chr6:99564147
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0002g0220 | 2 | HG01070.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.33-1199C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564147 | ||||||
chr6:99564153
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0140 | 6 | HG02723.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-1205C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564153 | ||||||
chr6:99564221
|
T | G | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-1273A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564221 | ||||||
chr6:99564237
|
C | T | 9 | a0001c0001t0002g0005a0001c0001t0002g0021a0001c0001t0002g0215others(6): Show | 23 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-1289G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564237 | ||||||
chr6:99564273
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.33-1325T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564273 | ||||||
chr6:99564422
|
C | CA | 26 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0024others(23): Show | 45 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.33-1475dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564422 | ||||||
chr6:99564422
|
CA | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0019others(83): Show | 142 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.33-1475delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564422 | ||||||
chr6:99564422
|
CAA | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0073others(10): Show | 30 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.33-1476_33-1475del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564422 | ||||||
chr6:99564450
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.33-1502T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564450 | ||||||
chr6:99564517
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.33-1569G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564517 | ||||||
chr6:99564647
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-1699C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564647 | ||||||
chr6:99564723
|
CAA | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0147 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-1777_33-1776del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564723 | ||||||
chr6:99564809
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.33-1861C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564809 | ||||||
chr6:99565065
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.33-2117C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565065 | ||||||
chr6:99565079
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.33-2131A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565079 | ||||||
chr6:99565316
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-2368C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565316 | ||||||
chr6:99565348
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2400T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565348 | ||||||
chr6:99565386
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2438C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565386 | ||||||
chr6:99565388
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2440A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565388 | ||||||
chr6:99565389
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2441T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565389 | ||||||
chr6:99565390
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2442T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565390 | ||||||
chr6:99565500
|
T | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(80): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.33-2552A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565500 | ||||||
chr6:99565529
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-2581C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565529 | ||||||
chr6:99565590
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.33-2642T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565590 | ||||||
chr6:99565817
|
A | G | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.32+2679T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565817 | ||||||
chr6:99566110
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0173 | 5 | NA18941.hp2 NA18964.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+2386A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566110 | ||||||
chr6:99566130
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32+2366G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566130 | ||||||
chr6:99566268
|
GTCTT | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.32+2224_32+2227del others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566268 | ||||||
chr6:99566277
|
T | C | 1 | a0001c0001t0001g0025 | 3 | HG02559.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.32+2219A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566277 | ||||||
chr6:99566444
|
T | G | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+2052A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566444 | ||||||
chr6:99566586
|
C | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+1910G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566586 | ||||||
chr6:99566956
|
C | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+1540G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566956 | ||||||
chr6:99567022
|
G | C | 1 | a0001c0001t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.32+1474C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567022 | ||||||
chr6:99567042
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.32+1454A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567042 | ||||||
chr6:99567194
|
TA | T | 35 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(32): Show | 67 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.32+1301delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567194 | ||||||
chr6:99567244
|
GCTT | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0028others(22): Show | 44 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+1249_32+1251del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567244 | ||||||
chr6:99567388
|
CACACACA others(13): Show |
C | 2 | a0001c0001t0001g0017a0001c0001t0008g0088 | 5 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+1088_32+1107del others(20): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567388 | ||||||
chr6:99567408
|
T | TAC | 2 | a0001c0001t0001g0043a0001c0001t0001g0203 | 3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.32+1086_32+1087dup others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567408 | ||||||
chr6:99567420
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 7 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+1076G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567420 | ||||||
chr6:99567428
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0086others(5): Show | 12 | HG01099.hp1 HG02630.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+1068A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567428 | ||||||
chr6:99567428
|
T | TAC | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.32+1066_32+1067dup others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567428 | ||||||
chr6:99567428
|
T | TACAC | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02602.hp1 NA18959.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.32+1064_32+1067dup others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567428 | ||||||
chr6:99567540
|
T | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 7 | HG01099.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+956A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567540 | ||||||
chr6:99567631
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+865C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567631 | ||||||
chr6:99567681
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+815T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567681 | ||||||
chr6:99567691
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32+805A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567691 | ||||||
chr6:99567721
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.32+775T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567721 | ||||||
chr6:99568076
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+420C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568076 | ||||||
chr6:99568239
|
C | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+257G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568239 | ||||||
chr6:99568319
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.32+177C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568319 | ||||||
chr6:99568364
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.32+132T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568364 | ||||||
chr6:99568464
|
G | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0021a0001c0001t0002g0215others(8): Show | 25 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.32+32C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568464 | ||||||
chr6:99568486
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0224 | 3 | NA19011.hp2 NA19081.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.32+10C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568486 |