Item | Value |
---|---|
geneid | 1539 |
ensemblid | ENSG00000155833.15 |
hgncid | 2583 |
symbol | CYLC2 |
name | cylicin 2 |
refseq_nuc | NM_001340.5 |
refseq_prot | NP_001331.1 |
ensembl_nuc | ENST00000374798.8 |
ensembl_prot | ENSP00000420256.1 |
mane_status | MANE Select |
chr | chr9 |
start | 102995333 |
end | 103018488 |
strand | + |
ver | v1.2 |
region | chr9:102995333-103018488 |
region5000 | chr9:102990333-103023488 |
regionname0 | CYLC2_chr9_102995333_103018488 |
regionname5000 | CYLC2_chr9_102990333_103023488 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 348 | 392 | 83 | 82 | 173 | 9 | 43 | 145 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0002 | 0/0 | 348 | 36 | 0 | 0 | 34 | 1 | 1 | 21 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0003 | 0/0 | 344 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(339): Show |
chr9 | 102990333 | 103023488 |
a0004 | 0/0 | 348 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0005 | 0/0 | 348 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0006 | 0/0 | 348 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0007 | 0/0 | 344 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(339): Show |
chr9 | 102990333 | 103023488 |
a0008 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0009 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0010 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0011 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0012 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0013 | 0/0 | 348 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
a0014 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | MSLPR others(343): Show |
chr9 | 102990333 | 103023488 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1044 | 390 | 81 | 82 | 173 | 9 | 43 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0001c0005 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0002c0002 | 0/0 | 1044 | 36 | 0 | 0 | 34 | 1 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0003c0003 | 0/0 | 1032 | 4 | 3 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1027): Show |
chr9 | 102990333 | 103023488 | ||
a0004c0004 | 0/0 | 1044 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0005c0008 | 0/0 | 1044 | 2 | 1 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0006c0007 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0007c0006 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1027): Show |
chr9 | 102990333 | 103023488 | ||
a0008c0011 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0009c0013 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0010c0010 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0011c0009 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0012c0012 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0013c0014 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 | ||
a0014c0015 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | ATGTC others(1039): Show |
chr9 | 102990333 | 103023488 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2137 | 50 | 6 | 7 | 27 | 0 | 10 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0002 | 0/1 | 2131 | 53 | 6 | 11 | 30 | 3 | 2 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2126): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0003 | 0/0 | 2157 | 24 | 6 | 0 | 17 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2152): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0004 | 0/0 | 2155 | 23 | 1 | 0 | 21 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2150): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0005 | 0/0 | 2153 | 22 | 2 | 7 | 10 | 0 | 3 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2148): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0006 | 0/0 | 2135 | 22 | 6 | 5 | 10 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2130): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0007 | 0/0 | 2139 | 21 | 1 | 8 | 7 | 0 | 5 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2134): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0008 | 0/0 | 2159 | 20 | 0 | 5 | 11 | 0 | 4 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2154): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0009 | 0/0 | 2151 | 13 | 1 | 3 | 6 | 0 | 3 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2146): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0011 | 0/0 | 2151 | 13 | 3 | 3 | 4 | 0 | 3 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2146): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0012 | 0/0 | 2147 | 11 | 9 | 1 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2142): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0013 | 0/0 | 2161 | 7 | 0 | 3 | 3 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2156): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0014 | 0/0 | 2145 | 9 | 3 | 4 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2140): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0016 | 0/0 | 2141 | 8 | 1 | 0 | 4 | 1 | 2 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2136): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0018 | 0/0 | 2151 | 7 | 3 | 3 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2146): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0019 | 0/0 | 2145 | 7 | 3 | 3 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2140): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0020 | 0/0 | 2143 | 7 | 3 | 2 | 1 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2138): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0021 | 0/0 | 2149 | 6 | 1 | 3 | 1 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2144): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0022 | 0/0 | 2143 | 6 | 3 | 1 | 0 | 1 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2138): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0024 | 0/0 | 2163 | 3 | 0 | 1 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2158): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0025 | 0/0 | 2149 | 5 | 1 | 0 | 3 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2144): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0026 | 0/0 | 2133 | 5 | 1 | 1 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2128): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0027 | 0/0 | 2157 | 4 | 4 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2152): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0028 | 0/0 | 2153 | 4 | 1 | 2 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2148): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0029 | 0/0 | 2129 | 4 | 0 | 0 | 4 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2124): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0031 | 0/0 | 2153 | 3 | 0 | 0 | 1 | 0 | 2 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2148): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0032 | 1/0 | 2149 | 3 | 0 | 2 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2144): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0033 | 0/0 | 2149 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2144): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0035 | 0/0 | 2155 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2150): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0036 | 0/0 | 2155 | 2 | 1 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2150): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0037 | 0/0 | 2147 | 2 | 1 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2142): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0038 | 0/0 | 2137 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0041 | 0/0 | 2141 | 2 | 1 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2136): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0042 | 0/0 | 2153 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2148): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0045 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2164): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0046 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2162): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0047 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2160): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0048 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2158): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0049 | 0/0 | 2157 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2152): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0050 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2146): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0051 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2134): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0052 | 0/0 | 2135 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2130): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0053 | 0/0 | 2131 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2126): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0054 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2122): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0055 | 0/0 | 2146 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2141): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0056 | 0/0 | 2144 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2139): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0060 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2152): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0061 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2140): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0062 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2140): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0063 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2134): Show |
chr9 | 102990333 | 103023488 |
a0001c0001t0064 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2129): Show |
chr9 | 102990333 | 103023488 |
a0001c0005t0040 | 0/0 | 2140 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2135): Show |
chr9 | 102990333 | 103023488 |
a0002c0002t0010 | 0/0 | 2139 | 13 | 0 | 0 | 12 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2134): Show |
chr9 | 102990333 | 103023488 |
a0002c0002t0015 | 0/0 | 2141 | 8 | 0 | 0 | 8 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2136): Show |
chr9 | 102990333 | 103023488 |
a0002c0002t0017 | 0/0 | 2125 | 7 | 0 | 0 | 7 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2120): Show |
chr9 | 102990333 | 103023488 |
a0002c0002t0023 | 0/0 | 2137 | 5 | 0 | 0 | 5 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
a0002c0002t0030 | 0/0 | 2143 | 3 | 0 | 0 | 2 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2138): Show |
chr9 | 102990333 | 103023488 |
a0003c0003t0034 | 0/0 | 2137 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
a0003c0003t0043 | 0/0 | 2135 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2130): Show |
chr9 | 102990333 | 103023488 |
a0003c0003t0044 | 0/0 | 2133 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2128): Show |
chr9 | 102990333 | 103023488 |
a0004c0004t0009 | 0/0 | 2151 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2146): Show |
chr9 | 102990333 | 103023488 |
a0005c0008t0013 | 0/0 | 2161 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2156): Show |
chr9 | 102990333 | 103023488 |
a0005c0008t0024 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2158): Show |
chr9 | 102990333 | 103023488 |
a0006c0007t0058 | 0/0 | 2141 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2136): Show |
chr9 | 102990333 | 103023488 |
a0006c0007t0059 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2134): Show |
chr9 | 102990333 | 103023488 |
a0007c0006t0039 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2110): Show |
chr9 | 102990333 | 103023488 |
a0008c0011t0024 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2158): Show |
chr9 | 102990333 | 103023488 |
a0009c0013t0001 | 0/0 | 2137 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
a0010c0010t0013 | 0/0 | 2161 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2156): Show |
chr9 | 102990333 | 103023488 |
a0011c0009t0001 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
a0012c0012t0057 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2129): Show |
chr9 | 102990333 | 103023488 |
a0013c0014t0033 | 0/0 | 2149 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2144): Show |
chr9 | 102990333 | 103023488 |
a0014c0015t0001 | 0/0 | 2137 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | AGTTT others(2132): Show |
chr9 | 102990333 | 103023488 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0003 | 0/0 | 8 | 0 | 3 | 2 | 2 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0002g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0001 | 0/0 | 9 | 4 | 0 | 5 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0001 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0004 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0001 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0009g0001 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0009g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0009g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0005 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0011g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0012g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0012g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0012g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0013g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0013g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0013g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0016g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0016g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0016g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0016g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0018g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0018g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0018g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0018g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0018g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0019g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0019g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0019g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0019g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0019g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0020g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0020g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0020g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0021g0005 | 0/0 | 5 | 1 | 2 | 1 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0021g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0022g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0022g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0024g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0024g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0024g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0025g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0025g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0025g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0025g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0025g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0026g0003 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0026g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0026g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0026g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0027g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0027g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0027g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0027g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0028g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0028g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0028g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0028g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0029g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0029g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0029g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0031g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0031g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0031g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0032g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0032g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0032g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0033g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0035g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0035g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0036g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0036g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0037g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0037g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0038g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0038g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0041g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0042g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0045g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0046g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0047g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0048g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0049g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0050g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0051g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0052g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0053g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0054g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0055g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0056g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0060g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0061g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0062g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0063g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0001t0064g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0005t0040g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0001c0005t0040g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0015g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0015g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0015g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0015g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0017g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0017g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0017g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0023g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0023g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0023g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0023g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0030g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0002c0002t0030g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0003c0003t0034g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0003c0003t0034g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0003c0003t0043g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0003c0003t0044g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0004c0004t0009g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0005c0008t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0005c0008t0024g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0006c0007t0058g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0006c0007t0059g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0007c0006t0039g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0008c0011t0024g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0009c0013t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0010c0010t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0011c0009t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0012c0012t0057g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0013c0014t0033g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
a0014c0015t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00140 | hp2 | a0001 | c0001 | t0021 | g0005 | EUR | GBR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | FIN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00280 | hp2 | a0001 | c0001 | t0019 | g0219 | EUR | FIN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00323 | hp1 | a0002 | c0002 | t0010 | g0222 | EUR | FIN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00323 | hp2 | a0001 | c0001 | t0022 | g0015 | EUR | FIN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00423 | hp2 | a0002 | c0002 | t0023 | g0225 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00438 | hp2 | a0002 | c0002 | t0023 | g0006 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00621 | hp1 | a0002 | c0002 | t0017 | g0101 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00639 | hp1 | a0001 | c0001 | t0018 | g0031 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00642 | hp1 | a0001 | c0001 | t0019 | g0015 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0151 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00673 | hp1 | a0002 | c0002 | t0015 | g0223 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00673 | hp2 | a0001 | c0001 | t0029 | g0003 | EAS | CHS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00735 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00738 | hp1 | a0001 | c0001 | t0032 | g0060 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG00741 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0149 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01070 | hp2 | a0001 | c0001 | t0024 | g0187 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0186 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01081 | hp1 | a0001 | c0001 | t0019 | g0060 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01081 | hp2 | a0001 | c0001 | t0018 | g0206 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01109 | hp2 | a0003 | c0003 | t0044 | g0168 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01167 | hp1 | a0001 | c0001 | t0011 | g0005 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0026 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01168 | hp1 | a0001 | c0001 | t0037 | g0059 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01168 | hp2 | a0001 | c0001 | t0019 | g0015 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01169 | hp1 | a0001 | c0001 | t0032 | g0059 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01169 | hp2 | a0001 | c0001 | t0014 | g0026 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0157 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01192 | hp2 | a0001 | c0001 | t0028 | g0215 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01243 | hp1 | a0001 | c0001 | t0036 | g0214 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01243 | hp2 | a0001 | c0001 | t0014 | g0026 | AMR | PUR | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01255 | hp1 | a0001 | c0001 | t0028 | g0211 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01255 | hp2 | a0001 | c0001 | t0026 | g0116 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01256 | hp1 | a0001 | c0001 | t0048 | g0001 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01256 | hp2 | a0001 | c0001 | t0013 | g0039 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01257 | hp1 | a0001 | c0001 | t0020 | g0047 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01258 | hp1 | a0001 | c0001 | t0020 | g0047 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0039 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01261 | hp1 | a0001 | c0001 | t0021 | g0005 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01261 | hp2 | a0001 | c0001 | t0013 | g0001 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01346 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01358 | hp2 | a0001 | c0001 | t0042 | g0004 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01361 | hp1 | a0001 | c0001 | t0014 | g0154 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01361 | hp2 | a0005 | c0008 | t0024 | g0189 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01496 | hp1 | a0001 | c0001 | t0022 | g0015 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01496 | hp2 | a0001 | c0001 | t0011 | g0077 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01517 | hp1 | a0001 | c0001 | t0016 | g0159 | EUR | IBS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01517 | hp2 | a0001 | c0001 | t0028 | g0031 | EUR | IBS | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0161 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0058 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01891 | hp2 | a0001 | c0001 | t0037 | g0209 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01928 | hp2 | a0001 | c0001 | t0021 | g0005 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0072 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01943 | hp1 | a0001 | c0001 | t0011 | g0005 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01952 | hp1 | a0001 | c0001 | t0041 | g0030 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01952 | hp2 | a0001 | c0001 | t0018 | g0031 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01975 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01981 | hp1 | a0001 | c0001 | t0021 | g0080 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01981 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01993 | hp2 | a0001 | c0001 | t0054 | g0138 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02015 | hp1 | a0002 | c0002 | t0017 | g0038 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02015 | hp2 | a0008 | c0011 | t0024 | g0172 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02027 | hp1 | a0002 | c0002 | t0017 | g0017 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02027 | hp2 | a0009 | c0013 | t0001 | g0002 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02055 | hp1 | a0001 | c0001 | t0019 | g0074 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02055 | hp2 | a0001 | c0001 | t0019 | g0220 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02056 | hp1 | a0001 | c0001 | t0025 | g0014 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02071 | hp2 | a0001 | c0001 | t0026 | g0125 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02074 | hp1 | a0002 | c0002 | t0015 | g0232 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02074 | hp2 | a0001 | c0001 | t0026 | g0009 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02080 | hp1 | a0002 | c0002 | t0015 | g0011 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02080 | hp2 | a0001 | c0001 | t0045 | g0014 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02083 | hp2 | a0002 | c0002 | t0017 | g0017 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02129 | hp2 | a0001 | c0001 | t0035 | g0088 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02132 | hp1 | a0002 | c0002 | t0015 | g0226 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02145 | hp1 | a0001 | c0001 | t0011 | g0083 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02148 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02155 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | CDX | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02155 | hp2 | a0002 | c0002 | t0017 | g0017 | EAS | CDX | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02165 | hp1 | a0002 | c0002 | t0030 | g0006 | EAS | CDX | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02165 | hp2 | a0001 | c0001 | t0024 | g0192 | EAS | CDX | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02257 | hp1 | a0001 | c0001 | t0038 | g0204 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02257 | hp2 | a0001 | c0001 | t0028 | g0208 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02258 | hp1 | a0001 | c0001 | t0061 | g0076 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02280 | hp2 | a0001 | c0001 | t0025 | g0175 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0070 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02451 | hp2 | a0001 | c0001 | t0022 | g0217 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02523 | hp1 | a0010 | c0010 | t0013 | g0001 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02523 | hp2 | a0002 | c0002 | t0017 | g0017 | EAS | KHV | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02572 | hp1 | a0001 | c0001 | t0056 | g0055 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02572 | hp2 | a0001 | c0001 | t0026 | g0003 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02602 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02615 | hp1 | a0006 | c0007 | t0059 | g0164 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02622 | hp1 | a0001 | c0001 | t0050 | g0079 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02630 | hp2 | a0001 | c0001 | t0027 | g0212 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02647 | hp1 | a0011 | c0009 | t0001 | g0108 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02698 | hp1 | a0001 | c0001 | t0009 | g0174 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02717 | hp1 | a0001 | c0001 | t0041 | g0030 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02717 | hp2 | a0001 | c0001 | t0036 | g0210 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02723 | hp1 | a0001 | c0001 | t0055 | g0055 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02723 | hp2 | a0007 | c0006 | t0039 | g0035 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02735 | hp2 | a0001 | c0001 | t0053 | g0001 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02809 | hp1 | a0012 | c0012 | t0057 | g0200 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02809 | hp2 | a0001 | c0001 | t0060 | g0021 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02886 | hp1 | a0007 | c0006 | t0039 | g0035 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02886 | hp2 | a0001 | c0001 | t0014 | g0158 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02895 | hp1 | a0001 | c0001 | t0011 | g0034 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02895 | hp2 | a0001 | c0001 | t0027 | g0216 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02896 | hp1 | a0001 | c0001 | t0062 | g0203 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0028 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0034 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02922 | hp2 | a0001 | c0001 | t0063 | g0030 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02965 | hp2 | a0001 | c0001 | t0020 | g0049 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02976 | hp1 | a0003 | c0003 | t0034 | g0169 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03017 | hp1 | a0001 | c0001 | t0011 | g0085 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03017 | hp2 | a0001 | c0001 | t0008 | g0051 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03098 | hp1 | a0006 | c0007 | t0058 | g0165 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03098 | hp2 | a0003 | c0003 | t0034 | g0170 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03130 | hp1 | a0001 | c0001 | t0018 | g0207 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03130 | hp2 | a0001 | c0001 | t0052 | g0057 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03195 | hp2 | a0003 | c0003 | t0043 | g0167 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0166 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0144 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03453 | hp1 | a0013 | c0014 | t0033 | g0021 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03453 | hp2 | a0001 | c0001 | t0020 | g0049 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03486 | hp1 | a0001 | c0001 | t0033 | g0021 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0148 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0044 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03491 | hp2 | a0001 | c0001 | t0016 | g0008 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03492 | hp2 | a0001 | c0001 | t0016 | g0008 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | ESN | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03540 | hp2 | a0001 | c0001 | t0019 | g0205 | AFR | GWD | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03654 | hp1 | a0001 | c0001 | t0007 | g0042 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03704 | hp1 | a0001 | c0001 | t0049 | g0179 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0048 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03710 | hp2 | a0001 | c0001 | t0022 | g0015 | SAS | PJL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03831 | hp1 | a0001 | c0001 | t0011 | g0082 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03831 | hp2 | a0001 | c0001 | t0020 | g0050 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03834 | hp1 | a0001 | c0001 | t0007 | g0176 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03834 | hp2 | a0001 | c0001 | t0031 | g0084 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03927 | hp1 | a0002 | c0002 | t0030 | g0227 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0182 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0048 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0181 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04184 | hp1 | a0001 | c0001 | t0031 | g0086 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04199 | hp1 | a0001 | c0001 | t0025 | g0178 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04204 | hp1 | a0001 | c0001 | t0008 | g0194 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04204 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG04228 | hp2 | a0001 | c0001 | t0013 | g0001 | SAS | STU | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18522 | hp1 | a0001 | c0001 | t0018 | g0058 | AFR | YRI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18906 | hp1 | a0001 | c0005 | t0040 | g0163 | AFR | YRI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18906 | hp2 | a0001 | c0001 | t0022 | g0221 | AFR | YRI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18943 | hp1 | a0001 | c0001 | t0025 | g0013 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18945 | hp2 | a0004 | c0004 | t0009 | g0032 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18946 | hp1 | a0002 | c0002 | t0010 | g0061 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18949 | hp1 | a0001 | c0001 | t0026 | g0003 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18951 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18956 | hp2 | a0001 | c0001 | t0016 | g0152 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18961 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18962 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18963 | hp1 | a0002 | c0002 | t0023 | g0011 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18963 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18966 | hp2 | a0001 | c0001 | t0012 | g0068 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18968 | hp1 | a0001 | c0001 | t0013 | g0014 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18970 | hp1 | a0002 | c0002 | t0010 | g0230 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18971 | hp1 | a0002 | c0002 | t0023 | g0011 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18972 | hp1 | a0001 | c0001 | t0014 | g0073 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18975 | hp1 | a0002 | c0002 | t0010 | g0033 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18977 | hp1 | a0002 | c0002 | t0010 | g0006 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18979 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18979 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18981 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18981 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18982 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18982 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18983 | hp1 | a0002 | c0002 | t0010 | g0061 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18984 | hp2 | a0001 | c0001 | t0024 | g0188 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18985 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18986 | hp1 | a0001 | c0001 | t0009 | g0184 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18986 | hp2 | a0002 | c0002 | t0015 | g0011 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18988 | hp1 | a0002 | c0002 | t0010 | g0011 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18989 | hp1 | a0001 | c0001 | t0047 | g0053 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18989 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18990 | hp1 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18990 | hp2 | a0002 | c0002 | t0010 | g0011 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18991 | hp2 | a0001 | c0001 | t0025 | g0069 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18992 | hp2 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18994 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18994 | hp2 | a0001 | c0001 | t0031 | g0078 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18995 | hp2 | a0002 | c0002 | t0010 | g0033 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18997 | hp2 | a0014 | c0015 | t0001 | g0089 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18999 | hp1 | a0001 | c0001 | t0029 | g0003 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19000 | hp1 | a0001 | c0001 | t0035 | g0087 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19001 | hp1 | a0002 | c0002 | t0015 | g0006 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19002 | hp2 | a0001 | c0001 | t0029 | g0141 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19003 | hp1 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19003 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19005 | hp1 | a0002 | c0002 | t0010 | g0228 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19006 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19006 | hp2 | a0002 | c0002 | t0023 | g0231 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19007 | hp2 | a0004 | c0004 | t0009 | g0032 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19009 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19009 | hp2 | a0002 | c0002 | t0015 | g0006 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19011 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19012 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19030 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | LWK | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | LWK | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19043 | hp2 | a0001 | c0001 | t0038 | g0057 | AFR | LWK | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19054 | hp1 | a0002 | c0002 | t0017 | g0038 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19057 | hp2 | a0002 | c0002 | t0030 | g0006 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19058 | hp1 | a0001 | c0001 | t0008 | g0198 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19060 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19062 | hp1 | a0002 | c0002 | t0010 | g0033 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19063 | hp1 | a0001 | c0001 | t0008 | g0052 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19063 | hp2 | a0001 | c0001 | t0046 | g0053 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19066 | hp1 | a0002 | c0002 | t0010 | g0229 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19070 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19074 | hp1 | a0002 | c0002 | t0010 | g0224 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19075 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19075 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19076 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19078 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19079 | hp1 | a0004 | c0004 | t0009 | g0032 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19081 | hp2 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19083 | hp2 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19085 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19089 | hp1 | a0001 | c0001 | t0029 | g0124 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19089 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19090 | hp1 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0218 | AFR | YRI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0096 | AFR | ASW | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20805 | hp2 | a0001 | c0001 | t0018 | g0063 | EUR | TSI | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0007 | SAS | GIH | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01123 | hp1 | a0001 | c0001 | t0051 | g0007 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0028 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG02559 | hp2 | a0005 | c0008 | t0013 | g0001 | AFR | ACB | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03471 | hp1 | a0001 | c0001 | t0033 | g0021 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG03471 | hp2 | a0001 | c0005 | t0040 | g0162 | AFR | MSL | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | USA | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0155 | AFR | USA | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18955 | hp1 | a0002 | c0002 | t0015 | g0006 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA18955 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20300 | hp1 | a0001 | c0001 | t0021 | g0005 | AFR | USA | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | USA | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA21309 | hp1 | a0001 | c0001 | t0064 | g0202 | AFR | LWK | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
NA21309 | hp2 | a0001 | c0001 | t0027 | g0213 | AFR | LWK | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0146 | REF | REF | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
homoSapiens | grch38p0 | a0001 | c0001 | t0032 | g0062 | REF | REF | CYLC2_chr9_102990333_103023488 | CYLC2 | chr9 | 102990333 | 103023488 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:103003183 | G | A | 1 | a0011 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/8 | 148/2149 | 100/1047 | 34/348 | chr9 | 103003183 | |||
chr9:103005052 | T | G | 1 | a0010 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.421T>G | p.Ser141Ala | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 469/2149 | 421/1047 | 141/348 | chr9 | 103005052 | |||
chr9:103005067 | G | T | 1 | a0005 | 2 | HG01361.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.436G>T | p.Asp146Tyr | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 484/2149 | 436/1047 | 146/348 | chr9 | 103005067 | |||
chr9:103005122 | G | T | 1 | a0006 | 2 | HG02615.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.491G>T | p.Gly164Val | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 539/2149 | 491/1047 | 164/348 | chr9 | 103005122 | |||
chr9:103005179 | G | A | 1 | a0008 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.548G>A | p.Gly183Glu | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 596/2149 | 548/1047 | 183/348 | chr9 | 103005179 | |||
chr9:103005199 | A | G | 2 | a0002 a0004 |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
missense_variant | MODERATE | c.568A>G | p.Lys190Glu | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 616/2149 | 568/1047 | 190/348 | chr9 | 103005199 | |||
chr9:103005254 | G | A | 2 | a0002 a0004 |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
missense_variant | MODERATE | c.623G>A | p.Gly208Asp | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 671/2149 | 623/1047 | 208/348 | chr9 | 103005254 | |||
chr9:103005263 | G | C | 1 | a0012 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.632G>C | p.Gly211Ala | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 680/2149 | 632/1047 | 211/348 | chr9 | 103005263 | |||
chr9:103005311 | G | A | 1 | a0009 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.680G>A | p.Gly227Asp | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 728/2149 | 680/1047 | 227/348 | chr9 | 103005311 | |||
chr9:103005474 | C | G | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.843C>G | p.Asp281Glu | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 891/2149 | 843/1047 | 281/348 | chr9 | 103005474 | |||
chr9:103005521 | C | T | 1 | a0013 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.890C>T | p.Thr297Met | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 938/2149 | 890/1047 | 297/348 | chr9 | 103005521 | |||
chr9:103005527 | ATGCCAAG others(5): Show |
A | 1 | a0007 | 2 | HG02723.hp2 HG02886.hp1 |
disruptive_inframe_deletion | MODERATE | c.908_919delTTGCCAAG others(4): Show |
p.Val303_Lys306del | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 956/2149 | 908/1047 | 303/348 | INFO_REALIGN_3_PRIME | chr9 | 103005527 | ||
chr9:103005587 | C | A | 1 | a0002 | 36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
missense_variant | MODERATE | c.956C>A | p.Ala319Glu | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 1004/2149 | 956/1047 | 319/348 | chr9 | 103005587 | |||
chr9:103005600 | TAAGAAGG others(5): Show |
T | 1 | a0003 | 4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
conservative_inframe_deletion | MODERATE | c.988_999delGATGCAAA others(4): Show |
p.Asp330_Lys333del | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 1036/2149 | 988/1047 | 330/348 | INFO_REALIGN_3_PRIME | chr9 | 103005600 | ||
chr9:103018325 | G | A | 2 | a0001 a0012 |
6 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
splice_region_variant | LOW | c.*891G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 8/8 | chr9 | 103018325 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:103001602 | T | C | 1 | a0001c0005 | 2 | HG03471.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.42T>C | p.Tyr14Tyr | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/8 | 90/2149 | 42/1047 | 14/348 | chr9 | 103001602 | |||
chr9:103005420 | T | C | 2 | a0002c0002 a0004c0004 |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
synonymous_variant | LOW | c.789T>C | p.Asp263Asp | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 837/2149 | 789/1047 | 263/348 | chr9 | 103005420 | |||
chr9:103005516 | C | T | 1 | a0002c0002 | 36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
synonymous_variant | LOW | c.885C>T | p.Asp295Asp | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 933/2149 | 885/1047 | 295/348 | chr9 | 103005516 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:102995356 | T | A | 1 | a0001c0001t0042 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/8 | 25 | chr9 | 102995356 | ||||||
chr9:103005705 | G | T | 1 | a0001c0001t0064 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 27 | chr9 | 103005705 | ||||||
chr9:103005744 | G | A | 3 | a0003c0003t0034 a0003c0003t0043 a0003c0003t0044 |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*66G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 66 | chr9 | 103005744 | ||||||
chr9:103005890 | A | T | 7 | a0001c0001t0033 a0001c0001t0041 a0001c0001t0060 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*212A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 212 | chr9 | 103005890 | ||||||
chr9:103005920 | T | A | 5 | a0002c0002t0010 a0002c0002t0015 a0002c0002t0017 others(2): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*242T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 242 | chr9 | 103005920 | ||||||
chr9:103005945 | G | A | 5 | a0002c0002t0010 a0002c0002t0015 a0002c0002t0017 others(2): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 267 | chr9 | 103005945 | ||||||
chr9:103005961 | G | T | 2 | a0006c0007t0058 a0006c0007t0059 |
2 | HG02615.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*283G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 283 | chr9 | 103005961 | ||||||
chr9:103005966 | AAAG | A | 5 | a0001c0001t0055 a0001c0001t0056 a0001c0001t0064 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*294_*296delGAA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 294 | INFO_REALIGN_3_PRIME | chr9 | 103005966 | |||||
chr9:103006017 | G | GAC | 5 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0018 others(2): Show |
37 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*394dupCA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACAC | 4 | a0001c0001t0005 a0001c0001t0028 a0001c0001t0031 others(1): Show |
30 | HG00741.hp1 HG01099.hp2 HG01192.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*391_*394dupCACA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACAC | 3 | a0001c0001t0004 a0001c0001t0035 a0001c0001t0036 |
27 | HG00621.hp2 HG01243.hp1 HG02083.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*389_*394dupCACACA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(1): Show |
4 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0049 others(1): Show |
30 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*387_*394dupCACACA others(2): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(3): Show |
1 | a0001c0001t0008 | 20 | HG00609.hp2 HG00741.hp2 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*385_*394dupCACACA others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(5): Show |
3 | a0001c0001t0013 a0005c0008t0013 a0010c0010t0013 |
9 | HG01256.hp2 HG01258.hp2 HG01261.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*383_*394dupCACACA others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(7): Show |
4 | a0001c0001t0024 a0001c0001t0048 a0005c0008t0024 others(1): Show |
6 | HG01070.hp2 HG01256.hp1 HG01361.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*381_*394dupCACACA others(8): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(9): Show |
1 | a0001c0001t0047 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379_*394dupCACACA others(10): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(11): Show |
1 | a0001c0001t0046 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*377_*394dupCACACA others(12): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | G | GACACACA others(13): Show |
1 | a0001c0001t0045 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*375_*394dupCACACA others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GAC | G | 4 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0056 others(1): Show |
15 | HG01069.hp2 HG01168.hp1 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*394delCA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 393 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACAC | G | 5 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0061 others(2): Show |
19 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*391_*394delCACA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 391 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACAC | G | 4 | a0001c0001t0020 a0001c0001t0022 a0001c0005t0040 others(1): Show |
18 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*389_*394delCACACA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 389 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(1): Show |
G | 4 | a0001c0001t0016 a0001c0001t0041 a0002c0002t0015 others(1): Show |
19 | HG00673.hp1 HG01517.hp1 HG01952.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*387_*394delCACACA others(2): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 387 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(3): Show |
G | 5 | a0001c0001t0007 a0001c0001t0051 a0001c0001t0063 others(2): Show |
37 | HG00323.hp1 HG00733.hp2 HG01123.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*385_*394delCACACA others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 385 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(5): Show |
G | 8 | a0001c0001t0001 a0001c0001t0038 a0001c0001t0064 others(5): Show |
62 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*383_*394delCACACA others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 383 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(7): Show |
G | 2 | a0001c0001t0006 a0001c0001t0052 |
23 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*381_*394delCACACA others(8): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 381 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(9): Show |
G | 1 | a0001c0001t0026 | 5 | HG01255.hp2 HG02071.hp2 HG02074.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*379_*394delCACACA others(10): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 379 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(11): Show |
G | 2 | a0001c0001t0002 a0001c0001t0053 |
53 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*377_*394delCACACA others(12): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 377 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(13): Show |
G | 1 | a0001c0001t0029 | 4 | HG00673.hp2 NA18999.hp1 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*394delCACACA others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 375 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(15): Show |
G | 2 | a0001c0001t0054 a0007c0006t0039 |
3 | HG01993.hp2 HG02723.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373_*394delCACACA others(16): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 373 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006017 | GACACACA others(17): Show |
G | 1 | a0002c0002t0017 | 7 | HG00621.hp1 HG02015.hp1 HG02027.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*394delCACACA others(18): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 371 | INFO_REALIGN_3_PRIME | chr9 | 103006017 | |||||
chr9:103006073 | G | C | 3 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0031 |
9 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 395 | chr9 | 103006073 | ||||||
chr9:103006163 | T | G | 2 | a0003c0003t0043 a0003c0003t0044 |
2 | HG01109.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*485T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 485 | chr9 | 103006163 | ||||||
chr9:103006175 | G | A | 1 | a0007c0006t0039 | 2 | HG02723.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*497G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 497 | chr9 | 103006175 | ||||||
chr9:103006193 | T | C | 1 | a0001c0001t0050 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 515 | chr9 | 103006193 | ||||||
chr9:103006221 | T | C | 5 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0031 others(2): Show |
25 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*543T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 543 | chr9 | 103006221 | ||||||
chr9:103006257 | G | C | 7 | a0001c0001t0033 a0001c0001t0041 a0001c0001t0060 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*579G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 579 | chr9 | 103006257 | ||||||
chr9:103006295 | A | G | 5 | a0002c0002t0010 a0002c0002t0015 a0002c0002t0017 others(2): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*617A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 617 | chr9 | 103006295 | ||||||
chr9:103006317 | C | A | 2 | a0001c0001t0048 a0001c0001t0053 |
2 | HG01256.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*639C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 639 | chr9 | 103006317 | ||||||
chr9:103006373 | C | T | 4 | a0001c0001t0062 a0003c0003t0034 a0003c0003t0043 others(1): Show |
5 | HG01109.hp2 HG02896.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*695C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/8 | 695 | chr9 | 103006373 | ||||||
chr9:103018334 | G | A | 1 | a0001c0001t0051 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*900G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 8/8 | 12656 | chr9 | 103018334 | ||||||
chr9:103018336 | G | A | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*902G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 8/8 | 12658 | chr9 | 103018336 | ||||||
chr9:103018353 | C | T | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*919C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 8/8 | 12675 | chr9 | 103018353 | ||||||
chr9:103018480 | G | C | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*1046G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 8/8 | 12802 | chr9 | 103018480 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:102995474 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(287): Show |
445 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(442): Show |
intron_variant | MODIFIER | c.17+77A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995474 | |||||||
chr9:102995484 | T | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.17+87T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995484 | |||||||
chr9:102995659 | A | AT | 20 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(17): Show |
31 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.17+269dupT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 102995659 | ||||||
chr9:102995748 | A | AT | 20 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(17): Show |
31 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.17+357dupT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 102995748 | ||||||
chr9:102995759 | A | C | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+362A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995759 | |||||||
chr9:102995847 | T | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0067 a0001c0001t0007g0007 others(11): Show |
20 | HG01123.hp1 HG01934.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.17+450T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995847 | |||||||
chr9:102995872 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.17+475G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995872 | |||||||
chr9:102995920 | G | A | 1 | a0001c0001t0019g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.17+523G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995920 | |||||||
chr9:102995942 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.17+545G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102995942 | |||||||
chr9:102996023 | T | C | 1 | a0001c0001t0061g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.17+626T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996023 | |||||||
chr9:102996095 | C | A | 17 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(14): Show |
28 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.17+698C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996095 | |||||||
chr9:102996109 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
13 | HG00438.hp1 NA18612.hp2 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.17+712T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996109 | |||||||
chr9:102996142 | AAAATAAA others(15): Show |
A | 1 | a0001c0001t0014g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.17+747_17+768delAA others(20): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 102996142 | ||||||
chr9:102996168 | C | T | 2 | a0001c0001t0035g0087 a0001c0001t0035g0088 |
2 | HG02129.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.17+771C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996168 | |||||||
chr9:102996192 | A | C | 1 | a0001c0001t0007g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.17+795A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996192 | |||||||
chr9:102996195 | C | A | 94 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(91): Show |
147 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.17+798C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996195 | |||||||
chr9:102996195 | C | T | 1 | a0001c0001t0007g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.17+798C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996195 | |||||||
chr9:102996196 | A | AGTTTCTA others(43): Show |
1 | a0001c0001t0007g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.17+799_17+800insGT others(48): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996196 | |||||||
chr9:102996258 | T | C | 1 | a0001c0001t0005g0143 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.17+861T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996258 | |||||||
chr9:102996380 | T | C | 17 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(14): Show |
28 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.17+983T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996380 | |||||||
chr9:102996412 | A | G | 3 | a0001c0001t0041g0030 a0001c0001t0062g0203 a0001c0001t0063g0030 |
4 | HG01952.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+1015A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996412 | |||||||
chr9:102996454 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.17+1057A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996454 | |||||||
chr9:102996569 | A | G | 1 | a0001c0001t0002g0046 | 2 | NA18969.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.17+1172A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996569 | |||||||
chr9:102996751 | T | G | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.17+1354T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996751 | |||||||
chr9:102996764 | T | G | 1 | a0001c0001t0011g0077 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.17+1367T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996764 | |||||||
chr9:102996839 | A | G | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+1442A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996839 | |||||||
chr9:102996907 | C | T | 11 | a0001c0001t0019g0015 a0001c0001t0019g0060 a0001c0001t0019g0219 others(8): Show |
14 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.17+1510C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996907 | |||||||
chr9:102996950 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0020g0047 |
3 | HG01123.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.17+1553G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102996950 | |||||||
chr9:102997024 | T | C | 15 | a0001c0001t0019g0015 a0001c0001t0019g0060 a0001c0001t0019g0205 others(12): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.17+1627T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997024 | |||||||
chr9:102997034 | G | A | 2 | a0001c0001t0009g0048 a0001c0001t0014g0026 |
5 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.17+1637G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997034 | |||||||
chr9:102997157 | A | G | 5 | a0001c0001t0007g0008 a0001c0001t0007g0070 a0001c0001t0007g0071 others(2): Show |
9 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.17+1760A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997157 | |||||||
chr9:102997162 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(36): Show |
64 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.17+1765G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997162 | |||||||
chr9:102997202 | G | A | 17 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(14): Show |
28 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.17+1805G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997202 | |||||||
chr9:102997269 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.17+1872T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997269 | |||||||
chr9:102997289 | G | C | 16 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(13): Show |
26 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.17+1892G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997289 | |||||||
chr9:102997362 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(257): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.17+1965A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997362 | |||||||
chr9:102997372 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(255): Show |
408 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(405): Show |
intron_variant | MODIFIER | c.17+1975T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997372 | |||||||
chr9:102997380 | T | G | 2 | a0001c0005t0040g0162 a0001c0005t0040g0163 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.17+1983T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997380 | |||||||
chr9:102997525 | T | G | 1 | a0002c0002t0015g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.17+2128T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997525 | |||||||
chr9:102997528 | A | C | 4 | a0001c0001t0033g0021 a0001c0001t0060g0021 a0001c0001t0061g0076 others(1): Show |
5 | HG02258.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.17+2131A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997528 | |||||||
chr9:102997565 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(108): Show |
179 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.17+2168A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997565 | |||||||
chr9:102997731 | T | A | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+2334T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997731 | |||||||
chr9:102997818 | T | A | 1 | a0001c0001t0031g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.17+2421T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997818 | |||||||
chr9:102997915 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.17+2518T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102997915 | |||||||
chr9:102998044 | T | C | 1 | a0001c0001t0014g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.17+2647T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998044 | |||||||
chr9:102998061 | A | G | 1 | a0001c0001t0016g0159 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.17+2664A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998061 | |||||||
chr9:102998099 | A | G | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+2702A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998099 | |||||||
chr9:102998135 | G | T | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+2738G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998135 | |||||||
chr9:102998268 | C | T | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+2871C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998268 | |||||||
chr9:102998411 | C | T | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.17+3014C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998411 | |||||||
chr9:102998458 | A | G | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+3061A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998458 | |||||||
chr9:102998510 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(253): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.18-3068A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998510 | |||||||
chr9:102998603 | C | A | 1 | a0001c0001t0018g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18-2975C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998603 | |||||||
chr9:102998612 | T | C | 4 | a0001c0001t0006g0022 a0001c0001t0006g0096 a0001c0001t0006g0097 others(1): Show |
6 | HG02615.hp2 HG02976.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-2966T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998612 | |||||||
chr9:102998625 | G | C | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18-2953G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998625 | |||||||
chr9:102998632 | T | C | 20 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(17): Show |
31 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.18-2946T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998632 | |||||||
chr9:102998652 | T | C | 1 | a0001c0001t0007g0066 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.18-2926T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998652 | |||||||
chr9:102998772 | T | C | 1 | a0001c0001t0007g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.18-2806T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102998772 | |||||||
chr9:102999071 | T | G | 1 | a0001c0001t0002g0099 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.18-2507T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999071 | |||||||
chr9:102999184 | G | T | 1 | a0001c0001t0029g0141 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.18-2394G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999184 | |||||||
chr9:102999208 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(213): Show |
344 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.18-2370T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999208 | |||||||
chr9:102999393 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.18-2185G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999393 | |||||||
chr9:102999608 | C | CTATCTAT others(52): Show |
1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.18-1968_18-1967ins others(59): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 102999608 | ||||||
chr9:102999856 | A | G | 1 | a0001c0001t0007g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.18-1722A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999856 | |||||||
chr9:102999898 | T | C | 1 | a0008c0011t0024g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.18-1680T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999898 | |||||||
chr9:102999935 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.18-1643C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 102999935 | |||||||
chr9:103000028 | G | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(210): Show |
337 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.18-1550G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000028 | |||||||
chr9:103000108 | G | C | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18-1470G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000108 | |||||||
chr9:103000199 | C | A | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.18-1379C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000199 | |||||||
chr9:103000237 | A | C | 1 | a0001c0001t0004g0056 | 2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.18-1341A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000237 | |||||||
chr9:103000337 | TTCTATTT others(6): Show |
T | 2 | a0001c0001t0018g0207 a0001c0001t0028g0208 |
2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.18-1226_18-1214del others(13): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 103000337 | ||||||
chr9:103000409 | G | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-1169G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000409 | |||||||
chr9:103000446 | G | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-1132G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000446 | |||||||
chr9:103000449 | T | A | 1 | a0001c0001t0014g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.18-1129T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000449 | |||||||
chr9:103000517 | T | C | 2 | a0001c0001t0004g0173 a0001c0001t0009g0174 |
2 | HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.18-1061T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000517 | |||||||
chr9:103000566 | T | A | 1 | a0001c0001t0014g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.18-1012T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000566 | |||||||
chr9:103000623 | A | G | 1 | a0001c0001t0035g0088 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.18-955A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000623 | |||||||
chr9:103000627 | C | CGAAAAAA others(45): Show |
1 | a0001c0001t0035g0088 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.18-941_18-940insTC others(50): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 103000627 | ||||||
chr9:103000642 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0201 |
2 | NA18949.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.18-936C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000642 | |||||||
chr9:103000654 | C | T | 4 | a0001c0001t0019g0205 a0001c0001t0038g0057 a0001c0001t0038g0204 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-924C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000654 | |||||||
chr9:103000721 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.18-857G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000721 | |||||||
chr9:103000725 | T | A | 1 | a0001c0001t0027g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18-853T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000725 | |||||||
chr9:103000741 | T | A | 1 | a0001c0001t0011g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.18-837T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000741 | |||||||
chr9:103000785 | C | T | 17 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(14): Show |
28 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.18-793C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000785 | |||||||
chr9:103000845 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.18-733G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000845 | |||||||
chr9:103000855 | T | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-723T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000855 | |||||||
chr9:103000911 | C | T | 2 | a0001c0001t0003g0029 a0001c0001t0004g0029 |
3 | HG01891.hp1 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.18-667C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103000911 | |||||||
chr9:103001019 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(206): Show |
335 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.18-559G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001019 | |||||||
chr9:103001136 | C | T | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.18-442C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001136 | |||||||
chr9:103001146 | A | C | 1 | a0001c0001t0022g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.18-432A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001146 | |||||||
chr9:103001209 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.18-369A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001209 | |||||||
chr9:103001289 | CA | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(257): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.18-287delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 103001289 | ||||||
chr9:103001342 | C | T | 14 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(11): Show |
24 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.18-236C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001342 | |||||||
chr9:103001468 | G | A | 21 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(18): Show |
32 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.18-110G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001468 | |||||||
chr9:103001530 | G | A | 3 | a0001c0001t0003g0012 a0001c0001t0004g0012 a0001c0001t0005g0012 |
5 | NA18944.hp1 NA18965.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.18-48G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | chr9 | 103001530 | |||||||
chr9:103001563 | TTTTTG | T | 13 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(10): Show |
22 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.18-10_18-6delGTTTT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 103001563 | ||||||
chr9:103001627 | G | A | 1 | a0001c0001t0025g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58+9G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001627 | |||||||
chr9:103001630 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(38): Show |
66 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.58+12T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001630 | |||||||
chr9:103001674 | T | C | 4 | a0001c0001t0033g0021 a0001c0001t0060g0021 a0001c0001t0061g0076 others(1): Show |
5 | HG02258.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+56T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001674 | |||||||
chr9:103001688 | C | CA | 13 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(10): Show |
22 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+73dupA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 103001688 | ||||||
chr9:103001817 | A | C | 7 | a0001c0001t0033g0021 a0001c0001t0041g0030 a0001c0001t0060g0021 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+199A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001817 | |||||||
chr9:103001834 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(102): Show |
173 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(170): Show |
intron_variant | MODIFIER | c.58+216T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001834 | |||||||
chr9:103001868 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.58+250A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001868 | |||||||
chr9:103001884 | T | C | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58+266T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103001884 | |||||||
chr9:103002042 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.58+424T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002042 | |||||||
chr9:103002100 | T | C | 2 | a0006c0007t0058g0165 a0006c0007t0059g0164 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.58+482T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002100 | |||||||
chr9:103002256 | C | T | 8 | a0001c0001t0003g0054 a0001c0001t0008g0014 a0001c0001t0008g0198 others(5): Show |
10 | HG02056.hp1 HG02080.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+638C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002256 | |||||||
chr9:103002324 | C | T | 1 | a0001c0001t0054g0138 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.58+706C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002324 | |||||||
chr9:103002357 | CT | C | 32 | a0001c0001t0012g0166 a0001c0001t0018g0031 a0001c0001t0018g0058 others(29): Show |
39 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-759delT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 103002357 | ||||||
chr9:103002357 | CTT | C | 45 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0092 others(42): Show |
60 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-760_59-759delTT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 103002357 | ||||||
chr9:103002357 | CTTT | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(175): Show |
298 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.59-761_59-759delTT others(1): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 103002357 | ||||||
chr9:103002357 | CTTTT | C | 26 | a0001c0001t0002g0023 a0001c0001t0002g0103 a0001c0001t0002g0104 others(23): Show |
39 | HG00140.hp2 HG01069.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+762_59-759delTT others(2): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 103002357 | ||||||
chr9:103002360 | T | C | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.58+742T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002360 | |||||||
chr9:103002361 | T | C | 2 | a0001c0001t0035g0087 a0001c0001t0050g0079 |
2 | HG02622.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.58+743T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002361 | |||||||
chr9:103002362 | T | C | 13 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(10): Show |
23 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.58+744T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002362 | |||||||
chr9:103002363 | T | C | 12 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(9): Show |
21 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.58+745T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002363 | |||||||
chr9:103002364 | T | C | 1 | a0001c0001t0031g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.58+746T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002364 | |||||||
chr9:103002524 | C | T | 24 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(21): Show |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-618C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002524 | |||||||
chr9:103002542 | C | T | 2 | a0002c0002t0015g0223 a0002c0002t0015g0232 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.59-600C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002542 | |||||||
chr9:103002544 | G | A | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-598G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002544 | |||||||
chr9:103002545 | G | T | 4 | a0001c0001t0006g0019 a0001c0001t0006g0025 a0001c0001t0006g0131 others(1): Show |
8 | NA18947.hp1 NA18959.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-597G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002545 | |||||||
chr9:103002547 | T | C | 1 | a0001c0001t0006g0096 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.59-595T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002547 | |||||||
chr9:103002566 | A | T | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-576A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002566 | |||||||
chr9:103002574 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(114): Show |
197 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(194): Show |
intron_variant | MODIFIER | c.59-568G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002574 | |||||||
chr9:103002627 | C | G | 1 | a0001c0001t0012g0068 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.59-515C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002627 | |||||||
chr9:103002647 | T | C | 1 | a0001c0001t0013g0039 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.59-495T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002647 | |||||||
chr9:103002688 | T | C | 7 | a0001c0001t0033g0021 a0001c0001t0041g0030 a0001c0001t0060g0021 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-454T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002688 | |||||||
chr9:103002754 | G | A | 24 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(21): Show |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-388G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002754 | |||||||
chr9:103002851 | G | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01257.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-291G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002851 | |||||||
chr9:103002853 | T | G | 1 | a0001c0001t0011g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.59-289T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002853 | |||||||
chr9:103002936 | C | T | 24 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(21): Show |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-206C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002936 | |||||||
chr9:103002952 | C | A | 1 | a0001c0001t0025g0178 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.59-190C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103002952 | |||||||
chr9:103003066 | G | A | 24 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(21): Show |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-76G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103003066 | |||||||
chr9:103003066 | G | T | 1 | a0001c0001t0008g0194 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.59-76G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 2/7 | chr9 | 103003066 | |||||||
chr9:103003328 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.180+65T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103003328 | |||||||
chr9:103003371 | A | C | 1 | a0001c0001t0064g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+108A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103003371 | |||||||
chr9:103003440 | G | A | 24 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(21): Show |
39 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.180+177G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103003440 | |||||||
chr9:103003636 | G | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+373G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103003636 | |||||||
chr9:103003922 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.180+659T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103003922 | |||||||
chr9:103003977 | A | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+714A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103003977 | |||||||
chr9:103004055 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181-640A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004055 | |||||||
chr9:103004197 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(113): Show |
196 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.181-498A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004197 | |||||||
chr9:103004267 | T | A | 18 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(15): Show |
29 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.181-428T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004267 | |||||||
chr9:103004284 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.181-411T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004284 | |||||||
chr9:103004289 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0016g0144 a0007c0006t0039g0035 |
4 | HG02723.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-406T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004289 | |||||||
chr9:103004296 | C | T | 14 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(11): Show |
23 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.181-399C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004296 | |||||||
chr9:103004355 | A | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(273): Show |
429 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(426): Show |
intron_variant | MODIFIER | c.181-340A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004355 | |||||||
chr9:103004444 | C | G | 1 | a0001c0001t0031g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.181-251C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004444 | |||||||
chr9:103004456 | G | A | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-239G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004456 | |||||||
chr9:103004631 | T | C | 1 | a0001c0001t0037g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.181-64T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 3/7 | chr9 | 103004631 | |||||||
chr9:103006402 | C | CTTATTTA others(9): Show |
3 | a0002c0002t0010g0228 a0002c0002t0023g0231 a0002c0002t0030g0227 |
3 | HG03927.hp1 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.*700+35_*700+50dup others(16): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103006402 | ||||||
chr9:103006402 | C | CTTATTTA others(13): Show |
7 | a0002c0002t0010g0006 a0002c0002t0010g0230 a0002c0002t0015g0006 others(4): Show |
11 | HG00438.hp2 HG02015.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.*700+31_*700+50dup others(20): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103006402 | ||||||
chr9:103006402 | C | CTTATTTA others(17): Show |
12 | a0002c0002t0010g0011 a0002c0002t0010g0033 a0002c0002t0010g0061 others(9): Show |
21 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.*700+27_*700+50dup others(24): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103006402 | ||||||
chr9:103006402 | CTTAT | C | 23 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(20): Show |
35 | HG00140.hp2 HG01109.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.*700+47_*700+50del others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103006402 | ||||||
chr9:103006406 | T | C | 1 | a0013c0014t0033g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*700+28T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006406 | |||||||
chr9:103006425 | ATTTT | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(201): Show |
326 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.*700+50_*700+53del others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103006425 | ||||||
chr9:103006429 | T | A | 2 | a0001c0001t0004g0040 a0001c0001t0012g0010 |
3 | HG02451.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.*700+51T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006429 | |||||||
chr9:103006438 | G | C | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+60G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006438 | |||||||
chr9:103006482 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*700+104C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006482 | |||||||
chr9:103006508 | G | T | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+130G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006508 | |||||||
chr9:103006518 | A | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(207): Show |
334 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.*700+140A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006518 | |||||||
chr9:103006546 | T | TG | 27 | a0001c0001t0001g0145 a0001c0001t0011g0005 a0001c0001t0011g0034 others(24): Show |
40 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.*700+170dupG | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103006546 | ||||||
chr9:103006549 | A | G | 1 | a0001c0001t0005g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*700+171A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006549 | |||||||
chr9:103006580 | A | T | 2 | a0001c0001t0032g0059 a0001c0001t0037g0059 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.*700+202A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006580 | |||||||
chr9:103006607 | G | A | 27 | a0001c0001t0001g0145 a0001c0001t0011g0005 a0001c0001t0011g0034 others(24): Show |
40 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.*700+229G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006607 | |||||||
chr9:103006626 | A | G | 27 | a0001c0001t0001g0145 a0001c0001t0011g0005 a0001c0001t0011g0034 others(24): Show |
40 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.*700+248A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006626 | |||||||
chr9:103006687 | T | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+309T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006687 | |||||||
chr9:103006703 | C | T | 1 | a0001c0001t0003g0054 | 2 | NA18939.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.*700+325C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006703 | |||||||
chr9:103006704 | G | A | 2 | a0001c0001t0041g0030 a0001c0001t0063g0030 |
3 | HG01952.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.*700+326G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006704 | |||||||
chr9:103006706 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*700+328G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006706 | |||||||
chr9:103006839 | T | G | 27 | a0001c0001t0001g0145 a0001c0001t0011g0005 a0001c0001t0011g0034 others(24): Show |
40 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.*700+461T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006839 | |||||||
chr9:103006843 | T | G | 27 | a0001c0001t0001g0145 a0001c0001t0011g0005 a0001c0001t0011g0034 others(24): Show |
40 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.*700+465T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006843 | |||||||
chr9:103006923 | C | T | 27 | a0001c0001t0001g0145 a0001c0001t0011g0005 a0001c0001t0011g0034 others(24): Show |
40 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.*700+545C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006923 | |||||||
chr9:103006924 | A | G | 1 | a0001c0001t0003g0193 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.*700+546A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103006924 | |||||||
chr9:103007012 | A | T | 4 | a0001c0001t0002g0100 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | NA18974.hp2 NA18992.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.*700+634A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007012 | |||||||
chr9:103007031 | T | C | 1 | a0001c0001t0011g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*700+653T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007031 | |||||||
chr9:103007036 | T | C | 7 | a0001c0001t0033g0021 a0001c0001t0041g0030 a0001c0001t0060g0021 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.*700+658T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007036 | |||||||
chr9:103007130 | A | C | 1 | a0001c0001t0022g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*700+752A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007130 | |||||||
chr9:103007167 | C | T | 2 | a0001c0001t0011g0085 a0001c0001t0031g0084 |
2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.*700+789C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007167 | |||||||
chr9:103007203 | C | T | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+825C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007203 | |||||||
chr9:103007246 | G | A | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*700+868G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007246 | |||||||
chr9:103007349 | A | T | 1 | a0001c0001t0027g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*700+971A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007349 | |||||||
chr9:103007351 | T | G | 1 | a0001c0001t0027g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*700+973T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007351 | |||||||
chr9:103007371 | A | G | 1 | a0001c0001t0027g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.*700+993A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007371 | |||||||
chr9:103007386 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(253): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.*700+1008A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007386 | |||||||
chr9:103007585 | A | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*700+1207A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007585 | |||||||
chr9:103007756 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(257): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.*700+1378C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007756 | |||||||
chr9:103007780 | T | A | 2 | a0003c0003t0043g0167 a0003c0003t0044g0168 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.*700+1402T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007780 | |||||||
chr9:103007786 | T | C | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+1408T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007786 | |||||||
chr9:103007787 | G | A | 1 | a0002c0002t0010g0229 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.*700+1409G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007787 | |||||||
chr9:103007874 | C | T | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+1496C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007874 | |||||||
chr9:103007876 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(257): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.*700+1498T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007876 | |||||||
chr9:103007926 | T | C | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*700+1548T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103007926 | |||||||
chr9:103007994 | C | CAAATCCT others(248): Show |
1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*700+1630_*700+163 others(259): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103007994 | ||||||
chr9:103007994 | C | CAAATCCT others(249): Show |
1 | a0001c0001t0016g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*700+1630_*700+163 others(260): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103007994 | ||||||
chr9:103008131 | C | G | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+1753C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008131 | |||||||
chr9:103008156 | TAA | T | 77 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(74): Show |
114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.*700+1782_*700+178 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103008156 | ||||||
chr9:103008160 | A | T | 1 | a0001c0001t0002g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*700+1782A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008160 | |||||||
chr9:103008163 | G | A | 77 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(74): Show |
114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.*700+1785G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008163 | |||||||
chr9:103008230 | G | A | 5 | a0001c0001t0002g0018 a0001c0001t0002g0041 a0001c0001t0002g0046 others(2): Show |
10 | HG01074.hp2 HG02040.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.*700+1852G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008230 | |||||||
chr9:103008274 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(230): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.*700+1896G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008274 | |||||||
chr9:103008311 | A | T | 1 | a0001c0001t0024g0192 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*700+1933A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008311 | |||||||
chr9:103008372 | TA | T | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*700+2000delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103008372 | ||||||
chr9:103008489 | C | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(253): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.*700+2111C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008489 | |||||||
chr9:103008497 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(253): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.*700+2119C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008497 | |||||||
chr9:103008565 | G | T | 1 | a0002c0002t0015g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*700+2187G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008565 | |||||||
chr9:103008593 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(230): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.*700+2215C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008593 | |||||||
chr9:103008637 | A | G | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*700+2259A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008637 | |||||||
chr9:103008670 | T | C | 1 | a0001c0001t0003g0180 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*700+2292T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008670 | |||||||
chr9:103008787 | C | A | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*700+2409C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008787 | |||||||
chr9:103008854 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(230): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.*700+2476G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103008854 | |||||||
chr9:103009168 | T | C | 2 | a0001c0001t0019g0074 a0001c0001t0050g0079 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.*700+2790T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009168 | |||||||
chr9:103009180 | A | G | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*700+2802A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009180 | |||||||
chr9:103009328 | C | A | 24 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(21): Show |
29 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.*701-2654C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009328 | |||||||
chr9:103009451 | G | A | 15 | a0001c0001t0019g0015 a0001c0001t0019g0060 a0001c0001t0019g0205 others(12): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.*701-2531G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009451 | |||||||
chr9:103009490 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(230): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.*701-2492C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009490 | |||||||
chr9:103009537 | C | G | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*701-2445C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009537 | |||||||
chr9:103009623 | T | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*701-2359T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009623 | |||||||
chr9:103009628 | T | C | 2 | a0002c0002t0015g0223 a0002c0002t0015g0232 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.*701-2354T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009628 | |||||||
chr9:103009640 | G | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*701-2342G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009640 | |||||||
chr9:103009783 | A | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(230): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.*701-2199A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009783 | |||||||
chr9:103009784 | G | A | 2 | a0001c0001t0019g0074 a0001c0001t0050g0079 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.*701-2198G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009784 | |||||||
chr9:103009793 | A | G | 1 | a0001c0001t0006g0131 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.*701-2189A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009793 | |||||||
chr9:103009835 | A | G | 1 | a0001c0001t0019g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*701-2147A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009835 | |||||||
chr9:103009906 | TACATATA others(32): Show |
T | 1 | a0011c0009t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.*701-2070_*701-203 others(43): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103009906 | ||||||
chr9:103009935 | G | GTATTATA others(12): Show |
6 | a0001c0001t0003g0001 a0001c0001t0003g0029 a0001c0001t0004g0029 others(3): Show |
11 | HG01074.hp1 HG01891.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.*701-2032_*701-203 others(23): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103009935 | ||||||
chr9:103009989 | GTA | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(224): Show |
364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.*701-1991_*701-199 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103009989 | ||||||
chr9:103009991 | A | G | 5 | a0001c0001t0001g0113 a0001c0001t0003g0191 a0001c0001t0003g0193 others(2): Show |
5 | HG01109.hp1 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.*701-1991A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009991 | |||||||
chr9:103009995 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0003g0191 a0001c0001t0003g0193 others(2): Show |
5 | HG01109.hp1 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.*701-1987G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009995 | |||||||
chr9:103009995 | GTA | G | 5 | a0002c0002t0010g0061 a0002c0002t0010g0224 a0002c0002t0010g0229 others(2): Show |
6 | HG01109.hp2 HG02132.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.*701-1972_*701-197 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103009995 | ||||||
chr9:103009997 | A | G | 1 | a0013c0014t0033g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*701-1985A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103009997 | |||||||
chr9:103010003 | A | G | 1 | a0001c0001t0003g0190 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.*701-1979A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010003 | |||||||
chr9:103010010 | T | C | 1 | a0001c0001t0027g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*701-1972T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010010 | |||||||
chr9:103010064 | T | C | 5 | a0001c0001t0018g0058 a0001c0001t0018g0207 a0001c0001t0028g0208 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.*701-1918T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010064 | |||||||
chr9:103010186 | T | C | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*701-1796T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010186 | |||||||
chr9:103010211 | T | C | 3 | a0001c0001t0003g0012 a0001c0001t0004g0012 a0001c0001t0005g0012 |
5 | NA18944.hp1 NA18965.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.*701-1771T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010211 | |||||||
chr9:103010275 | C | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*701-1707C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010275 | |||||||
chr9:103010307 | G | A | 2 | a0001c0001t0046g0053 a0001c0001t0047g0053 |
2 | NA18989.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.*701-1675G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010307 | |||||||
chr9:103010420 | C | A | 1 | a0001c0001t0064g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*701-1562C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010420 | |||||||
chr9:103010470 | A | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*701-1512A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010470 | |||||||
chr9:103010526 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(253): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.*701-1456T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010526 | |||||||
chr9:103010569 | G | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*701-1413G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010569 | |||||||
chr9:103010609 | A | G | 1 | a0001c0001t0003g0190 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.*701-1373A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010609 | |||||||
chr9:103010631 | C | A | 1 | a0001c0001t0006g0097 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*701-1351C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010631 | |||||||
chr9:103010696 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*701-1286T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010696 | |||||||
chr9:103010802 | CTCAG | C | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*701-1178_*701-117 others(8): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103010802 | ||||||
chr9:103010806 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(39): Show |
67 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.*701-1176G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010806 | |||||||
chr9:103010983 | A | G | 1 | a0001c0001t0004g0040 | 2 | NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.*701-999A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103010983 | |||||||
chr9:103011025 | A | T | 1 | a0001c0001t0011g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*701-957A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011025 | |||||||
chr9:103011137 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*701-845T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011137 | |||||||
chr9:103011227 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(253): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.*701-755G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011227 | |||||||
chr9:103011287 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*701-695C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011287 | |||||||
chr9:103011289 | C | A | 80 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(77): Show |
122 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.*701-693C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011289 | |||||||
chr9:103011341 | T | C | 1 | a0001c0001t0008g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.*701-641T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011341 | |||||||
chr9:103011348 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0112 others(1): Show |
4 | HG00735.hp2 HG01934.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.*701-634C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011348 | |||||||
chr9:103011355 | T | C | 2 | a0001c0001t0041g0030 a0001c0001t0063g0030 |
3 | HG01952.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.*701-627T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011355 | |||||||
chr9:103011361 | C | T | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*701-621C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011361 | |||||||
chr9:103011453 | T | C | 1 | a0001c0001t0027g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*701-529T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011453 | |||||||
chr9:103011555 | A | G | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*701-427A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011555 | |||||||
chr9:103011572 | A | T | 1 | a0005c0008t0024g0189 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.*701-410A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011572 | |||||||
chr9:103011600 | C | A | 1 | a0001c0001t0001g0036 | 2 | HG00438.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.*701-382C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011600 | |||||||
chr9:103011613 | T | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0103 a0001c0001t0002g0114 others(1): Show |
6 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.*701-369T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011613 | |||||||
chr9:103011628 | C | T | 1 | a0001c0001t0026g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.*701-354C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011628 | |||||||
chr9:103011663 | C | G | 1 | a0001c0001t0006g0096 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.*701-319C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011663 | |||||||
chr9:103011674 | T | C | 1 | a0001c0001t0011g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*701-308T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011674 | |||||||
chr9:103011713 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*701-269G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011713 | |||||||
chr9:103011805 | T | C | 1 | a0001c0001t0005g0182 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*701-177T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011805 | |||||||
chr9:103011825 | G | A | 101 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(98): Show |
145 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.*701-157G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011825 | |||||||
chr9:103011863 | A | G | 1 | a0001c0001t0029g0124 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.*701-119A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011863 | |||||||
chr9:103011942 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*701-40A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | chr9 | 103011942 | |||||||
chr9:103011947 | C | CT | 51 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(48): Show |
56 | HG00438.hp1 HG00621.hp2 HG00733.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.*701-8dupT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103011947 | ||||||
chr9:103011947 | C | CTT | 47 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0121 others(44): Show |
70 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.*701-9_*701-8dupTT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103011947 | ||||||
chr9:103011947 | C | CTTT | 12 | a0001c0001t0001g0115 a0001c0001t0001g0145 a0001c0001t0002g0003 others(9): Show |
14 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.*701-10_*701-8dupT others(2): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103011947 | ||||||
chr9:103011947 | CT | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(73): Show |
102 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(99): Show |
splice_region_variant&intron_variant | LOW | c.*701-8delT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103011947 | ||||||
chr9:103011947 | CTT | C | 44 | a0001c0001t0001g0002 a0001c0001t0002g0024 a0001c0001t0007g0008 others(41): Show |
56 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.*701-9_*701-8delTT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103011947 | ||||||
chr9:103011947 | CTTT | C | 5 | a0001c0001t0011g0005 a0001c0001t0019g0205 a0001c0001t0041g0030 others(2): Show |
6 | HG01167.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.*701-10_*701-8delT others(2): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 103011947 | ||||||
chr9:103012149 | T | A | 2 | a0001c0001t0003g0051 a0001c0001t0008g0051 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.*816+52T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012149 | |||||||
chr9:103012206 | T | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+109T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012206 | |||||||
chr9:103012211 | T | G | 1 | a0001c0001t0004g0183 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.*816+114T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012211 | |||||||
chr9:103012233 | T | C | 1 | a0001c0001t0025g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*816+136T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012233 | |||||||
chr9:103012240 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+143C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012240 | |||||||
chr9:103012305 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+208C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012305 | |||||||
chr9:103012419 | A | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(210): Show |
339 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.*816+322A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012419 | |||||||
chr9:103012503 | A | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(210): Show |
339 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.*816+406A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012503 | |||||||
chr9:103012504 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*816+407G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012504 | |||||||
chr9:103012678 | T | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+581T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012678 | |||||||
chr9:103012690 | A | T | 3 | a0001c0001t0038g0057 a0001c0001t0038g0204 a0001c0001t0052g0057 |
3 | HG02257.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.*816+593A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012690 | |||||||
chr9:103012741 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*816+644T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012741 | |||||||
chr9:103012892 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(257): Show |
410 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.*816+795A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012892 | |||||||
chr9:103012936 | G | A | 1 | a0001c0001t0029g0124 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.*816+839G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012936 | |||||||
chr9:103012990 | G | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+893G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103012990 | |||||||
chr9:103013003 | G | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*816+906G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013003 | |||||||
chr9:103013087 | T | C | 1 | a0001c0001t0009g0184 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.*816+990T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013087 | |||||||
chr9:103013127 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.*816+1030A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013127 | |||||||
chr9:103013153 | A | G | 1 | a0001c0001t0002g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.*816+1056A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013153 | |||||||
chr9:103013156 | T | TATATATT others(17): Show |
202 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(199): Show |
321 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.*816+1072_*816+109 others(28): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013156 | ||||||
chr9:103013156 | T | TATATATT others(41): Show |
3 | a0001c0001t0001g0142 a0001c0001t0012g0010 a0001c0001t0012g0166 |
8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.*816+1095_*816+109 others(52): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013156 | ||||||
chr9:103013168 | A | G | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1071A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013168 | |||||||
chr9:103013186 | T | TTATATAA others(12): Show |
1 | a0001c0001t0054g0138 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.*816+1095_*816+109 others(23): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013186 | ||||||
chr9:103013203 | A | G | 78 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(75): Show |
115 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.*816+1106A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013203 | |||||||
chr9:103013206 | T | A | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*816+1109T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013206 | |||||||
chr9:103013219 | T | G | 2 | a0003c0003t0043g0167 a0003c0003t0044g0168 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.*816+1122T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013219 | |||||||
chr9:103013238 | ACATGTAA others(26): Show |
A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1142_*816+117 others(37): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013238 | |||||||
chr9:103013251 | T | C | 1 | a0012c0012t0057g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*816+1154T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013251 | |||||||
chr9:103013261 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1164G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013261 | |||||||
chr9:103013262 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1165T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013262 | |||||||
chr9:103013262 | T | TTA | 14 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(11): Show |
22 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.*816+1173_*816+117 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013262 | ||||||
chr9:103013265 | T | TGTTTATA others(17): Show |
2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1168_*816+116 others(28): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013265 | |||||||
chr9:103013271 | T | A | 5 | a0001c0001t0003g0001 a0001c0001t0006g0022 a0001c0001t0006g0096 others(2): Show |
7 | HG02615.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.*816+1174T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013271 | |||||||
chr9:103013276 | T | TAATTATA others(112): Show |
2 | a0001c0001t0006g0151 a0001c0001t0006g0157 |
2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.*816+1180_*816+118 others(123): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013276 | ||||||
chr9:103013278 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1181T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013278 | |||||||
chr9:103013281 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1184C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013281 | |||||||
chr9:103013283 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1186C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013283 | |||||||
chr9:103013300 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1203C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013300 | |||||||
chr9:103013303 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1206G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013303 | |||||||
chr9:103013310 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1213G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013310 | |||||||
chr9:103013311 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1214T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013311 | |||||||
chr9:103013312 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1215T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013312 | |||||||
chr9:103013320 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1223C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013320 | |||||||
chr9:103013321 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1224C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013321 | |||||||
chr9:103013322 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+1225T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013322 | |||||||
chr9:103013322 | T | TATATATA others(29): Show |
76 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(73): Show |
116 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.*816+1234_*816+123 others(40): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(29): Show |
3 | a0001c0001t0006g0022 a0001c0001t0006g0097 a0001c0001t0006g0098 |
5 | HG02615.hp2 HG02976.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.*816+1234_*816+123 others(40): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(32): Show |
1 | a0001c0001t0036g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*816+1283_*816+132 others(43): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(30): Show |
2 | a0001c0005t0040g0162 a0001c0005t0040g0163 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*816+1236_*816+123 others(41): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(30): Show |
3 | a0006c0007t0058g0165 a0006c0007t0059g0164 a0012c0012t0057g0200 |
3 | HG02615.hp1 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*816+1236_*816+123 others(41): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(31): Show |
1 | a0001c0001t0064g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*816+1236_*816+123 others(42): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(29): Show |
75 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0012 others(72): Show |
132 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.*816+1236_*816+123 others(40): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | T | TATATATA others(68): Show |
1 | a0001c0001t0003g0185 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.*816+1236_*816+123 others(79): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013322 | TATATATA others(32): Show |
T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1283_*816+132 others(43): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013322 | ||||||
chr9:103013332 | TA | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(34): Show |
61 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.*816+1237delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013332 | ||||||
chr9:103013333 | A | AATATATT others(30): Show |
6 | a0001c0001t0033g0021 a0001c0001t0055g0055 a0001c0001t0056g0055 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.*816+1264_*816+126 others(41): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013333 | ||||||
chr9:103013333 | A | ATATATTA others(6): Show |
4 | a0001c0001t0005g0197 a0001c0001t0012g0028 a0001c0001t0014g0028 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*816+1236_*816+123 others(17): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013333 | |||||||
chr9:103013333 | A | ATATATTA others(28): Show |
2 | a0001c0001t0003g0052 a0001c0001t0008g0052 |
2 | NA18747.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.*816+1236_*816+123 others(39): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013333 | |||||||
chr9:103013344 | TA | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(116): Show |
185 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.*816+1250delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013344 | ||||||
chr9:103013346 | A | ATATAT | 4 | a0001c0001t0005g0197 a0001c0001t0012g0028 a0001c0001t0014g0028 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*816+1249_*816+125 others(9): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013346 | |||||||
chr9:103013348 | T | TTTA | 4 | a0001c0001t0005g0197 a0001c0001t0012g0028 a0001c0001t0014g0028 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*816+1251_*816+125 others(7): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013348 | |||||||
chr9:103013354 | TTATATAA others(3): Show |
T | 1 | a0001c0001t0002g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*816+1263_*816+127 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013354 | ||||||
chr9:103013356 | A | G | 1 | a0001c0001t0019g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*816+1259A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013356 | |||||||
chr9:103013359 | TA | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(33): Show |
60 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.*816+1265delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013359 | ||||||
chr9:103013360 | A | AATATATA others(28): Show |
2 | a0001c0001t0041g0030 a0001c0001t0063g0030 |
3 | HG01952.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.*816+1264_*816+126 others(39): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013360 | ||||||
chr9:103013360 | A | AATATATA others(28): Show |
1 | a0001c0001t0062g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*816+1264_*816+126 others(39): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013360 | ||||||
chr9:103013363 | T | C | 2 | a0003c0003t0043g0167 a0003c0003t0044g0168 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.*816+1266T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013363 | |||||||
chr9:103013365 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*816+1268T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013365 | |||||||
chr9:103013374 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.*816+1277T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013374 | |||||||
chr9:103013378 | T | C | 2 | a0001c0005t0040g0162 a0001c0005t0040g0163 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*816+1281T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013378 | |||||||
chr9:103013382 | A | G | 3 | a0001c0001t0006g0022 a0001c0001t0006g0097 a0001c0001t0006g0098 |
5 | HG02615.hp2 HG02976.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.*816+1285A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013382 | |||||||
chr9:103013398 | TA | T | 3 | a0001c0001t0001g0145 a0001c0001t0007g0106 a0001c0001t0016g0144 |
3 | HG03041.hp2 HG03209.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.*816+1304delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013398 | ||||||
chr9:103013425 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1328C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013425 | |||||||
chr9:103013464 | A | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1367A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013464 | |||||||
chr9:103013487 | C | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(273): Show |
429 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(426): Show |
intron_variant | MODIFIER | c.*816+1390C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013487 | |||||||
chr9:103013497 | A | G | 1 | a0001c0001t0027g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*816+1400A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013497 | |||||||
chr9:103013521 | T | A | 1 | a0001c0001t0027g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*816+1424T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013521 | |||||||
chr9:103013561 | G | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1464G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013561 | |||||||
chr9:103013575 | T | C | 1 | a0001c0001t0011g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*816+1478T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013575 | |||||||
chr9:103013613 | TATATA | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*816+1521_*816+152 others(9): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013613 | ||||||
chr9:103013615 | TATA | T | 3 | a0001c0001t0005g0197 a0001c0001t0012g0028 a0001c0001t0025g0175 |
4 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1522_*816+152 others(7): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013615 | ||||||
chr9:103013645 | TA | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*816+1553delA | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013645 | ||||||
chr9:103013654 | A | G | 1 | a0001c0001t0024g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.*816+1557A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013654 | |||||||
chr9:103013661 | T | A | 4 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0021g0005 others(1): Show |
8 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.*816+1564T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013661 | |||||||
chr9:103013686 | A | G | 14 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(11): Show |
23 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.*816+1589A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013686 | |||||||
chr9:103013688 | A | T | 1 | a0001c0001t0024g0187 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.*816+1591A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013688 | |||||||
chr9:103013690 | T | C | 1 | a0001c0001t0031g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*816+1593T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013690 | |||||||
chr9:103013730 | A | G | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*816+1633A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013730 | |||||||
chr9:103013752 | A | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0121 others(1): Show |
4 | HG02145.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.*816+1655A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013752 | |||||||
chr9:103013770 | T | C | 1 | a0001c0001t0061g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*816+1673T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013770 | |||||||
chr9:103013779 | TTA | T | 7 | a0001c0001t0033g0021 a0001c0001t0041g0030 a0001c0001t0060g0021 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.*816+1686_*816+168 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013779 | ||||||
chr9:103013828 | A | C | 1 | a0001c0001t0064g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*816+1731A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013828 | |||||||
chr9:103013836 | T | C | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1739T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013836 | |||||||
chr9:103013865 | T | TATATATT others(30): Show |
1 | a0001c0001t0006g0025 | 3 | NA18979.hp2 NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.*816+1773_*816+180 others(41): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013865 | ||||||
chr9:103013866 | A | ATATATTA others(33): Show |
11 | a0001c0001t0019g0015 a0001c0001t0019g0060 a0001c0001t0019g0219 others(8): Show |
14 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.*816+1782_*816+182 others(44): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013866 | ||||||
chr9:103013885 | A | G | 12 | a0001c0001t0003g0013 a0001c0001t0003g0054 a0001c0001t0005g0013 others(9): Show |
16 | HG01943.hp2 HG01978.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.*816+1788A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013885 | |||||||
chr9:103013892 | T | C | 2 | a0001c0001t0002g0104 a0001c0001t0007g0070 |
2 | HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.*816+1795T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013892 | |||||||
chr9:103013899 | TATA | T | 4 | a0001c0001t0012g0010 a0001c0001t0012g0166 a0001c0001t0055g0055 others(1): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.*816+1806_*816+180 others(7): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013899 | ||||||
chr9:103013968 | A | G | 1 | a0001c0001t0013g0039 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.*816+1871A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013968 | |||||||
chr9:103013979 | T | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1882T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013979 | |||||||
chr9:103013986 | TATG | T | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*816+1892_*816+189 others(7): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103013986 | ||||||
chr9:103013989 | G | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1892G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013989 | |||||||
chr9:103013996 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+1899C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103013996 | |||||||
chr9:103014029 | A | AT | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*816+1933dupT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014029 | ||||||
chr9:103014089 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*816+1992T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014089 | |||||||
chr9:103014105 | TAATA | T | 7 | a0001c0001t0001g0067 a0001c0001t0002g0104 a0001c0001t0007g0008 others(4): Show |
11 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.*816+2013_*816+201 others(8): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014105 | ||||||
chr9:103014128 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*816+2031T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014128 | |||||||
chr9:103014139 | T | C | 2 | a0006c0007t0058g0165 a0006c0007t0059g0164 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*816+2042T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014139 | |||||||
chr9:103014143 | T | C | 77 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0012 others(74): Show |
134 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.*816+2046T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014143 | |||||||
chr9:103014151 | T | TTAATATA others(27): Show |
4 | a0001c0001t0002g0105 a0001c0001t0009g0174 a0001c0005t0040g0162 others(1): Show |
4 | HG01978.hp2 HG02698.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+2102_*816+213 others(38): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014151 | ||||||
chr9:103014151 | T | TTAATATA others(61): Show |
1 | a0001c0001t0064g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*816+2068_*816+213 others(72): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014151 | ||||||
chr9:103014151 | TTAATATA others(27): Show |
T | 3 | a0001c0001t0014g0148 a0001c0001t0014g0158 a0001c0001t0020g0049 |
4 | HG02886.hp2 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+2102_*816+213 others(38): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014151 | ||||||
chr9:103014180 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+2083C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014180 | |||||||
chr9:103014211 | T | C | 1 | a0001c0001t0008g0194 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*816+2114T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014211 | |||||||
chr9:103014214 | CATATATA | C | 7 | a0001c0001t0033g0021 a0001c0001t0041g0030 a0001c0001t0060g0021 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.*816+2132_*816+213 others(11): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014214 | ||||||
chr9:103014220 | T | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(21): Show |
29 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.*816+2123T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014220 | |||||||
chr9:103014229 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*816+2132A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014229 | |||||||
chr9:103014256 | TAATATAT others(7): Show |
T | 1 | a0001c0001t0024g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.*816+2172_*816+218 others(18): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014256 | ||||||
chr9:103014284 | G | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*816+2187G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014284 | |||||||
chr9:103014353 | T | A | 16 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(13): Show |
26 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.*816+2256T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014353 | |||||||
chr9:103014367 | A | G | 15 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(12): Show |
25 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.*816+2270A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014367 | |||||||
chr9:103014373 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*816+2276T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014373 | |||||||
chr9:103014384 | C | T | 4 | a0001c0001t0011g0082 a0001c0001t0011g0085 a0001c0001t0019g0220 others(1): Show |
4 | HG02055.hp2 HG03017.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.*816+2287C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014384 | |||||||
chr9:103014385 | G | A | 1 | a0001c0001t0031g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*816+2288G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014385 | |||||||
chr9:103014412 | A | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+2315A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014412 | |||||||
chr9:103014413 | TG | T | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*816+2317delG | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014413 | |||||||
chr9:103014414 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.*816+2317G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014414 | |||||||
chr9:103014418 | CATA | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(121): Show |
191 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.*816+2326_*816+232 others(7): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014418 | ||||||
chr9:103014421 | AATAACAT others(19): Show |
A | 79 | a0001c0001t0002g0075 a0001c0001t0003g0001 a0001c0001t0003g0004 others(76): Show |
136 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.*816+2326_*816+235 others(30): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014421 | ||||||
chr9:103014423 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0002g0120 a0012c0012t0057g0200 |
3 | HG01123.hp2 HG02809.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.*816+2326T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014423 | |||||||
chr9:103014424 | A | ATAATGTA others(13): Show |
3 | a0001c0001t0001g0147 a0001c0001t0002g0120 a0012c0012t0057g0200 |
3 | HG01123.hp2 HG02809.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.*816+2327_*816+232 others(24): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014424 | |||||||
chr9:103014439 | A | G | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*816+2342A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014439 | |||||||
chr9:103014441 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(167): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.*816+2344A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014441 | |||||||
chr9:103014448 | A | G | 1 | a0001c0001t0014g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.*816+2351A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014448 | |||||||
chr9:103014488 | T | C | 1 | a0001c0001t0026g0116 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.*816+2391T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014488 | |||||||
chr9:103014490 | CAATATAC others(11): Show |
C | 1 | a0001c0001t0008g0186 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.*817-2380_*817-236 others(22): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014490 | ||||||
chr9:103014505 | A | C | 1 | a0001c0001t0024g0192 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*817-2383A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014505 | |||||||
chr9:103014508 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*817-2380T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014508 | |||||||
chr9:103014518 | A | C | 1 | a0001c0001t0002g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*817-2370A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014518 | |||||||
chr9:103014524 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*817-2364T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014524 | |||||||
chr9:103014526 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-2362C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014526 | |||||||
chr9:103014528 | ATATACAT others(18): Show |
A | 12 | a0001c0001t0011g0034 a0001c0001t0018g0058 a0001c0001t0018g0206 others(9): Show |
14 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.*817-2253_*817-222 others(29): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014528 | ||||||
chr9:103014536 | C | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-2352C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014536 | |||||||
chr9:103014537 | ATATG | A | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*817-2347_*817-234 others(8): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014537 | ||||||
chr9:103014539 | ATGTATAT | A | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-2347_*817-234 others(11): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014539 | ||||||
chr9:103014549 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(182): Show |
306 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.*817-2339T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014549 | |||||||
chr9:103014553 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(203): Show |
327 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.*817-2335G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014553 | |||||||
chr9:103014574 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0036 others(195): Show |
321 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.*817-2314T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014574 | |||||||
chr9:103014578 | G | A | 5 | a0001c0001t0001g0130 a0003c0003t0034g0169 a0003c0003t0034g0170 others(2): Show |
5 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.*817-2310G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014578 | |||||||
chr9:103014599 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(208): Show |
337 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.*817-2289T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014599 | |||||||
chr9:103014610 | T | C | 3 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*817-2278T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014610 | |||||||
chr9:103014612 | ATATGTAT others(113): Show |
A | 2 | a0003c0003t0034g0169 a0003c0003t0034g0170 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*817-2260_*817-214 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014612 | ||||||
chr9:103014612 | ATATGTAT others(148): Show |
A | 2 | a0003c0003t0043g0167 a0003c0003t0044g0168 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.*817-2260_*817-210 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014612 | ||||||
chr9:103014624 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(167): Show |
273 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.*817-2264T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014624 | |||||||
chr9:103014631 | T | C | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*817-2257T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014631 | |||||||
chr9:103014635 | T | C | 7 | a0001c0001t0019g0015 a0001c0001t0019g0060 a0001c0001t0022g0217 others(4): Show |
8 | HG00738.hp1 HG01081.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.*817-2253T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014635 | |||||||
chr9:103014646 | T | G | 1 | a0001c0001t0011g0085 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*817-2242T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014646 | |||||||
chr9:103014649 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(44): Show |
72 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.*817-2239T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014649 | |||||||
chr9:103014653 | GTATACAC others(123): Show |
G | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*817-2228_*817-209 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014653 | ||||||
chr9:103014656 | T | C | 2 | a0001c0001t0012g0010 a0001c0001t0012g0166 |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.*817-2232T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014656 | |||||||
chr9:103014659 | A | ATATGTAA others(3): Show |
3 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*817-2229_*817-222 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014659 | |||||||
chr9:103014660 | C | A | 3 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*817-2228C>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014660 | |||||||
chr9:103014660 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(132): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.*817-2228C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014660 | |||||||
chr9:103014662 | A | G | 3 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*817-2226A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014662 | |||||||
chr9:103014674 | T | C | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-2214T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014674 | |||||||
chr9:103014678 | G | A | 3 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*817-2210G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014678 | |||||||
chr9:103014678 | G | GTATACAT others(28): Show |
2 | a0001c0001t0019g0015 a0001c0001t0027g0161 |
2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.*817-2061_*817-202 others(39): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014678 | ||||||
chr9:103014678 | GTATACAT others(63): Show |
G | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*817-2096_*817-202 others(74): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014678 | ||||||
chr9:103014678 | GTATACAT others(98): Show |
G | 114 | a0001c0001t0001g0110 a0001c0001t0002g0107 a0001c0001t0002g0119 others(111): Show |
185 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.*817-2131_*817-202 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014678 | ||||||
chr9:103014684 | ATATGTAA others(3): Show |
A | 3 | a0001c0005t0040g0162 a0001c0005t0040g0163 a0012c0012t0057g0200 |
3 | HG02809.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*817-2203_*817-219 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014684 | |||||||
chr9:103014684 | ATATGTAA others(73): Show |
A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(97): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.*817-2203_*817-212 others(84): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014684 | |||||||
chr9:103014685 | TATGTAAT others(3): Show |
T | 1 | a0001c0001t0001g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.*817-2202_*817-219 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014685 | |||||||
chr9:103014685 | TATGTAAT others(38): Show |
T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(28): Show |
42 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.*817-2202_*817-215 others(49): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014685 | |||||||
chr9:103014685 | TATGTAAT others(73): Show |
T | 1 | a0001c0001t0001g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*817-2202_*817-212 others(84): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014685 | |||||||
chr9:103014691 | A | T | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-2197A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014691 | |||||||
chr9:103014692 | T | A | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-2196T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014692 | |||||||
chr9:103014693 | A | T | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-2195A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014693 | |||||||
chr9:103014695 | A | C | 3 | a0001c0005t0040g0162 a0001c0005t0040g0163 a0012c0012t0057g0200 |
3 | HG02809.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*817-2193A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014695 | |||||||
chr9:103014697 | G | A | 4 | a0001c0001t0001g0130 a0001c0005t0040g0162 a0001c0005t0040g0163 others(1): Show |
4 | HG02809.hp1 HG03471.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.*817-2191G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014697 | |||||||
chr9:103014697 | G | GCAGTATA others(5): Show |
2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-2191_*817-219 others(16): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014697 | |||||||
chr9:103014713 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0055g0055 a0001c0001t0056g0055 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*817-2175A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014713 | |||||||
chr9:103014720 | TATGTAAT others(3): Show |
T | 3 | a0001c0001t0001g0130 a0001c0001t0055g0055 a0001c0001t0056g0055 |
3 | HG02572.hp1 HG02723.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*817-2167_*817-215 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014720 | |||||||
chr9:103014732 | G | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(31): Show |
45 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.*817-2156G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014732 | |||||||
chr9:103014746 | CAATATAC others(137): Show |
C | 3 | a0001c0001t0064g0202 a0002c0002t0015g0223 a0002c0002t0015g0232 |
3 | HG00673.hp1 HG02074.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*817-2131_*817-198 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014746 | ||||||
chr9:103014748 | A | G | 34 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(31): Show |
45 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.*817-2140A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014748 | |||||||
chr9:103014753 | C | CATAAT | 6 | a0001c0001t0003g0001 a0001c0001t0004g0173 a0001c0001t0005g0182 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.*817-2132_*817-213 others(9): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014753 | ||||||
chr9:103014754 | ATATGTAA others(3): Show |
A | 32 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(29): Show |
43 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.*817-2133_*817-212 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014754 | |||||||
chr9:103014755 | TATGTAAT others(3): Show |
T | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-2132_*817-212 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014755 | |||||||
chr9:103014756 | ATGTAATA others(118): Show |
A | 1 | a0002c0002t0017g0017 | 2 | HG02027.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.*817-2131_*817-200 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014756 | |||||||
chr9:103014765 | A | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(126): Show |
201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.*817-2123A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014765 | |||||||
chr9:103014766 | CG | C | 6 | a0001c0001t0003g0001 a0001c0001t0004g0173 a0001c0001t0005g0182 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.*817-2121delG | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014766 | |||||||
chr9:103014767 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(129): Show |
204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.*817-2121G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014767 | |||||||
chr9:103014776 | TTATGCAA others(81): Show |
T | 6 | a0001c0001t0003g0001 a0001c0001t0004g0173 a0001c0001t0005g0182 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.*817-2107_*817-202 others(92): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014776 | ||||||
chr9:103014781 | CAATATAC others(102): Show |
C | 3 | a0001c0005t0040g0162 a0001c0005t0040g0163 a0012c0012t0057g0200 |
3 | HG02809.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*817-2096_*817-198 others(4): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014781 | ||||||
chr9:103014783 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(129): Show |
204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.*817-2105A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014783 | |||||||
chr9:103014789 | ATATGTAA others(3): Show |
A | 3 | a0001c0001t0001g0065 a0001c0001t0055g0055 a0001c0001t0056g0055 |
3 | HG02572.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*817-2098_*817-208 others(14): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014789 | |||||||
chr9:103014800 | A | C | 3 | a0001c0001t0001g0065 a0001c0001t0055g0055 a0001c0001t0056g0055 |
3 | HG02572.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*817-2088A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014800 | |||||||
chr9:103014802 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0055g0055 a0001c0001t0056g0055 |
3 | HG02572.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*817-2086G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014802 | |||||||
chr9:103014818 | A | G | 3 | a0001c0001t0001g0065 a0001c0001t0055g0055 a0001c0001t0056g0055 |
3 | HG02572.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*817-2070A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014818 | |||||||
chr9:103014838 | T | G | 3 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 |
3 | HG02451.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*817-2050T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014838 | |||||||
chr9:103014858 | CATAAT | C | 3 | a0001c0001t0001g0065 a0001c0001t0055g0055 a0001c0001t0056g0055 |
3 | HG02572.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*817-2026_*817-202 others(9): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014858 | ||||||
chr9:103014859 | A | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(21): Show |
29 | HG00438.hp1 HG00733.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.*817-2029A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014859 | |||||||
chr9:103014864 | ATATGTAA others(14): Show |
A | 5 | a0001c0001t0033g0021 a0001c0001t0051g0007 a0001c0001t0060g0021 others(2): Show |
6 | HG01123.hp1 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*817-2011_*817-199 others(25): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103014864 | ||||||
chr9:103014890 | T | C | 2 | a0001c0001t0055g0055 a0001c0001t0056g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*817-1998T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014890 | |||||||
chr9:103014915 | C | T | 1 | a0012c0012t0057g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*817-1973C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103014915 | |||||||
chr9:103015000 | T | A | 2 | a0001c0005t0040g0162 a0001c0005t0040g0163 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*817-1888T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015000 | |||||||
chr9:103015034 | T | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0091 others(2): Show |
7 | HG00438.hp1 NA18944.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.*817-1854T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015034 | |||||||
chr9:103015077 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*817-1811T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015077 | |||||||
chr9:103015078 | A | AATATACA others(18): Show |
4 | a0001c0001t0028g0208 a0001c0001t0028g0211 a0001c0001t0036g0210 others(1): Show |
4 | HG01243.hp1 HG01255.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-1699_*817-167 others(29): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015078 | ||||||
chr9:103015078 | A | AATATACA others(43): Show |
1 | a0001c0001t0018g0058 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.*817-1724_*817-167 others(54): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015078 | ||||||
chr9:103015078 | A | AATATACA others(93): Show |
1 | a0001c0001t0018g0207 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.*817-1774_*817-167 others(104): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015078 | ||||||
chr9:103015078 | AATATACA others(18): Show |
A | 2 | a0001c0001t0018g0063 a0001c0001t0027g0213 |
2 | NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*817-1699_*817-167 others(29): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015078 | ||||||
chr9:103015078 | AATATACA others(68): Show |
A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(262): Show |
416 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(413): Show |
intron_variant | MODIFIER | c.*817-1749_*817-167 others(79): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015078 | ||||||
chr9:103015078 | AATATACA others(93): Show |
A | 8 | a0001c0001t0004g0183 a0001c0001t0005g0020 a0001c0001t0009g0020 others(5): Show |
10 | HG00323.hp1 HG01109.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.*817-1774_*817-167 others(104): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015078 | ||||||
chr9:103015161 | T | G | 1 | a0001c0001t0005g0143 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.*817-1727T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015161 | |||||||
chr9:103015197 | T | C | 1 | a0001c0001t0019g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*817-1691T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015197 | |||||||
chr9:103015222 | T | G | 2 | a0001c0005t0040g0162 a0001c0005t0040g0163 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*817-1666T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015222 | |||||||
chr9:103015228 | T | C | 1 | a0002c0002t0023g0225 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.*817-1660T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015228 | |||||||
chr9:103015281 | T | C | 1 | a0002c0002t0023g0225 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.*817-1607T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015281 | |||||||
chr9:103015281 | TATATA | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(43): Show |
71 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.*817-1599_*817-159 others(9): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015281 | ||||||
chr9:103015312 | T | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(39): Show |
67 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.*817-1576T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015312 | |||||||
chr9:103015367 | T | G | 4 | a0001c0001t0003g0195 a0001c0001t0004g0027 a0001c0001t0009g0027 others(1): Show |
4 | NA18964.hp2 NA18969.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-1521T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015367 | |||||||
chr9:103015386 | A | AAT | 12 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0082 others(9): Show |
21 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.*817-1491_*817-149 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015386 | ||||||
chr9:103015386 | A | C | 1 | a0001c0001t0004g0199 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.*817-1502A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015386 | |||||||
chr9:103015386 | AAT | A | 7 | a0001c0001t0022g0217 a0001c0001t0022g0218 a0001c0001t0022g0221 others(4): Show |
7 | HG01109.hp2 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.*817-1491_*817-149 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015386 | ||||||
chr9:103015391 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0016g0144 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.*817-1497A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015391 | |||||||
chr9:103015393 | A | ATAT | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*817-1494_*817-149 others(7): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015393 | ||||||
chr9:103015394 | T | C | 1 | a0001c0001t0038g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*817-1494T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015394 | |||||||
chr9:103015405 | T | G | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*817-1483T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015405 | |||||||
chr9:103015446 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0026g0125 |
2 | HG02071.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.*817-1442T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015446 | |||||||
chr9:103015497 | CAT | C | 7 | a0001c0001t0033g0021 a0001c0001t0041g0030 a0001c0001t0060g0021 others(4): Show |
9 | HG01952.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.*817-1387_*817-138 others(6): Show |
CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 103015497 | ||||||
chr9:103015568 | C | T | 4 | a0003c0003t0034g0169 a0003c0003t0034g0170 a0003c0003t0043g0167 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-1320C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015568 | |||||||
chr9:103015630 | T | C | 1 | a0001c0001t0049g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*817-1258T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015630 | |||||||
chr9:103015645 | C | G | 1 | a0001c0001t0050g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*817-1243C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015645 | |||||||
chr9:103015653 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*817-1235C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015653 | |||||||
chr9:103015657 | C | T | 1 | a0001c0001t0031g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*817-1231C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015657 | |||||||
chr9:103015738 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*817-1150T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015738 | |||||||
chr9:103015740 | T | G | 5 | a0001c0001t0061g0076 a0003c0003t0034g0169 a0003c0003t0034g0170 others(2): Show |
5 | HG01109.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.*817-1148T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015740 | |||||||
chr9:103015786 | T | A | 1 | a0001c0001t0019g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*817-1102T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015786 | |||||||
chr9:103015879 | G | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*817-1009G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015879 | |||||||
chr9:103015891 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(216): Show |
345 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.*817-997G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015891 | |||||||
chr9:103015989 | T | C | 1 | a0001c0001t0016g0152 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.*817-899T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103015989 | |||||||
chr9:103016226 | T | C | 17 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(14): Show |
27 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.*817-662T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016226 | |||||||
chr9:103016271 | A | G | 2 | a0001c0001t0041g0030 a0001c0001t0063g0030 |
3 | HG01952.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.*817-617A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016271 | |||||||
chr9:103016300 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.*817-588T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016300 | |||||||
chr9:103016355 | A | C | 14 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(11): Show |
23 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.*817-533A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016355 | |||||||
chr9:103016401 | T | C | 1 | a0001c0001t0022g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.*817-487T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016401 | |||||||
chr9:103016504 | C | T | 1 | a0001c0001t0027g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*817-384C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016504 | |||||||
chr9:103016508 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.*817-380G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016508 | |||||||
chr9:103016542 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*817-346G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016542 | |||||||
chr9:103016577 | G | A | 1 | a0001c0001t0006g0098 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*817-311G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016577 | |||||||
chr9:103016603 | A | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(210): Show |
339 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.*817-285A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016603 | |||||||
chr9:103016613 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*817-275T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016613 | |||||||
chr9:103016649 | A | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(283): Show |
440 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(437): Show |
intron_variant | MODIFIER | c.*817-239A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016649 | |||||||
chr9:103016673 | G | T | 1 | a0001c0001t0064g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*817-215G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016673 | |||||||
chr9:103016682 | A | G | 4 | a0001c0001t0019g0205 a0001c0001t0038g0057 a0001c0001t0038g0204 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-206A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016682 | |||||||
chr9:103016705 | T | G | 4 | a0001c0001t0019g0205 a0001c0001t0038g0057 a0001c0001t0038g0204 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.*817-183T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016705 | |||||||
chr9:103016826 | G | A | 1 | a0001c0001t0027g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*817-62G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016826 | |||||||
chr9:103016871 | C | G | 1 | a0001c0001t0007g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.*817-17C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 6/7 | chr9 | 103016871 | |||||||
chr9:103016962 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(258): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
splice_donor_variant&intron_variant | HIGH | c.*890+1G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103016962 | |||||||
chr9:103016987 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*890+26T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103016987 | |||||||
chr9:103017000 | T | C | 2 | a0006c0007t0058g0165 a0006c0007t0059g0164 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*890+39T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017000 | |||||||
chr9:103017040 | G | GT | 12 | a0001c0001t0002g0043 a0001c0001t0002g0118 a0001c0001t0006g0098 others(9): Show |
13 | HG01109.hp2 HG02615.hp1 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.*890+90dupT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 103017040 | ||||||
chr9:103017040 | GT | G | 28 | a0001c0001t0011g0005 a0001c0001t0011g0077 a0001c0001t0011g0081 others(25): Show |
40 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.*890+90delT | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 103017040 | ||||||
chr9:103017163 | G | A | 8 | a0001c0001t0019g0015 a0001c0001t0019g0060 a0001c0001t0019g0219 others(5): Show |
11 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.*890+202G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017163 | |||||||
chr9:103017194 | G | T | 8 | a0001c0001t0002g0009 a0001c0001t0002g0043 a0001c0001t0002g0100 others(5): Show |
13 | HG02074.hp2 NA18612.hp1 NA18962.hp1 others(10): Show |
intron_variant | MODIFIER | c.*890+233G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017194 | |||||||
chr9:103017198 | T | C | 1 | a0001c0001t0019g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*890+237T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017198 | |||||||
chr9:103017206 | G | A | 1 | a0001c0001t0002g0041 | 2 | NA18954.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.*890+245G>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017206 | |||||||
chr9:103017237 | A | G | 23 | a0002c0002t0010g0006 a0002c0002t0010g0011 a0002c0002t0010g0033 others(20): Show |
36 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.*890+276A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017237 | |||||||
chr9:103017289 | A | C | 2 | a0001c0001t0007g0132 a0001c0001t0020g0155 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*890+328A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017289 | |||||||
chr9:103017481 | A | G | 17 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(14): Show |
27 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.*890+520A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017481 | |||||||
chr9:103017587 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*890+626T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017587 | |||||||
chr9:103017616 | A | G | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*890+655A>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017616 | |||||||
chr9:103017634 | T | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*890+673T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017634 | |||||||
chr9:103017638 | T | C | 1 | a0007c0006t0039g0035 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.*890+677T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017638 | |||||||
chr9:103017991 | C | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*891-334C>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103017991 | |||||||
chr9:103018049 | T | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*891-276T>G | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018049 | |||||||
chr9:103018059 | A | T | 1 | a0003c0003t0034g0170 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.*891-266A>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018059 | |||||||
chr9:103018094 | G | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*891-231G>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018094 | |||||||
chr9:103018168 | A | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*891-157A>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018168 | |||||||
chr9:103018254 | C | T | 15 | a0001c0001t0011g0005 a0001c0001t0011g0034 a0001c0001t0011g0077 others(12): Show |
25 | HG00140.hp2 HG01167.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.*891-71C>T | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018254 | |||||||
chr9:103018276 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(211): Show |
340 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(337): Show |
intron_variant | MODIFIER | c.*891-49T>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018276 | |||||||
chr9:103018285 | G | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*891-40G>C | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018285 | |||||||
chr9:103018288 | T | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): Show |
341 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.*891-37T>A | CYLC2 | ENSG00000155833.15 | transcript | ENST00000374798.8 | protein_coding | 7/7 | chr9 | 103018288 |