Item | Value |
---|---|
geneid | 9342 |
ensemblid | ENSG00000099940.12 |
hgncid | 11133 |
symbol | SNAP29 |
name | synaptosome associated protein 29 |
refseq_nuc | NM_004782.4 |
refseq_prot | NP_004773.1 |
ensembl_nuc | ENST00000215730.12 |
ensembl_prot | ENSP00000215730.6 |
mane_status | MANE Select |
chr | chr22 |
start | 20859007 |
end | 20891214 |
strand | + |
ver | v1.2 |
region | chr22:20859007-20891214 |
region5000 | chr22:20854007-20896214 |
regionname0 | SNAP29_chr22_20859007_20891214 |
regionname5000 | SNAP29_chr22_20854007_20896214 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 258 | 362 | 89 | 75 | 142 | 12 | 42 | 110 | SNAP29_chr22_20854007_20896214 | SNAP29 | MSAYP others(253): Show |
chr22 | 20854007 | 20896214 |
a0002 | 0/0 | 258 | 17 | 0 | 3 | 14 | 0 | 0 | 10 | SNAP29_chr22_20854007_20896214 | SNAP29 | MSAYP others(253): Show |
chr22 | 20854007 | 20896214 |
a0003 | 0/0 | 258 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | MSAYP others(253): Show |
chr22 | 20854007 | 20896214 |
a0004 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | MSAYP others(253): Show |
chr22 | 20854007 | 20896214 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 774 | 225 | 70 | 40 | 86 | 7 | 21 | SNAP29_chr22_20854007_20896214 | SNAP29 | ATGTC others(769): Show |
chr22 | 20854007 | 20896214 | ||
a0001c0002 | 0/1 | 774 | 135 | 17 | 35 | 56 | 5 | 21 | SNAP29_chr22_20854007_20896214 | SNAP29 | ATGTC others(769): Show |
chr22 | 20854007 | 20896214 | ||
a0001c0005 | 0/0 | 774 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | ATGTC others(769): Show |
chr22 | 20854007 | 20896214 | ||
a0002c0003 | 0/0 | 774 | 17 | 0 | 3 | 14 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | ATGTC others(769): Show |
chr22 | 20854007 | 20896214 | ||
a0003c0004 | 0/0 | 774 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | ATGTC others(769): Show |
chr22 | 20854007 | 20896214 | ||
a0004c0006 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | ATGTC others(769): Show |
chr22 | 20854007 | 20896214 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4258 | 129 | 29 | 32 | 54 | 4 | 10 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0003 | 0/0 | 4258 | 24 | 2 | 4 | 12 | 0 | 6 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0007 | 0/0 | 4259 | 7 | 1 | 2 | 3 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0009 | 0/0 | 4238 | 7 | 1 | 0 | 6 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4233): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0013 | 0/0 | 4274 | 4 | 4 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4269): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0017 | 0/0 | 4258 | 4 | 3 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0020 | 0/0 | 4258 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0024 | 0/0 | 4259 | 2 | 1 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0025 | 0/0 | 4258 | 2 | 0 | 0 | 0 | 2 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0026 | 0/0 | 4256 | 2 | 0 | 0 | 0 | 0 | 2 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4251): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0027 | 0/0 | 4260 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4255): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0029 | 0/0 | 4278 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4273): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0030 | 0/0 | 4272 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4267): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0031 | 0/0 | 4272 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4267): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0032 | 0/0 | 4264 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4259): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0034 | 0/0 | 4260 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4255): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0038 | 0/0 | 4258 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0039 | 0/0 | 4266 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4261): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0040 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0041 | 0/0 | 4251 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4246): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0042 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0043 | 1/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0044 | 0/0 | 4241 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4236): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0045 | 0/0 | 4260 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4255): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0046 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0047 | 0/0 | 4258 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0048 | 0/0 | 4258 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0049 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0050 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0051 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0053 | 0/0 | 4288 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4283): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0054 | 0/0 | 4280 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4275): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0055 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4273): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0056 | 0/0 | 4277 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4272): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0057 | 0/0 | 4276 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4271): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0058 | 0/0 | 4277 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4272): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0059 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4265): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0060 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4265): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0062 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4265): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0065 | 0/0 | 4263 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4258): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0066 | 0/0 | 4262 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4257): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0067 | 0/0 | 4260 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4255): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0076 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0078 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0001t0079 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0002 | 0/0 | 4259 | 42 | 1 | 17 | 15 | 3 | 6 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0004 | 0/0 | 4255 | 13 | 5 | 0 | 4 | 0 | 4 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4250): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0005 | 0/0 | 4247 | 11 | 2 | 5 | 3 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4242): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0006 | 0/0 | 4257 | 9 | 0 | 0 | 9 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4252): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0008 | 0/0 | 4261 | 8 | 0 | 4 | 4 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4256): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0011 | 0/0 | 4253 | 5 | 2 | 0 | 0 | 0 | 3 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4248): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0012 | 0/1 | 4251 | 5 | 0 | 0 | 1 | 0 | 3 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4246): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0014 | 0/0 | 4257 | 4 | 0 | 0 | 4 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4252): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0015 | 0/0 | 4249 | 4 | 0 | 2 | 1 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4244): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0016 | 0/0 | 4255 | 4 | 0 | 1 | 3 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4250): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0021 | 0/0 | 4263 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4258): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0022 | 0/0 | 4259 | 3 | 3 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0023 | 0/0 | 4247 | 3 | 0 | 1 | 0 | 1 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4242): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0033 | 0/0 | 4262 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4257): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0035 | 0/0 | 4257 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4252): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0036 | 0/0 | 4249 | 2 | 0 | 1 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4244): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0037 | 0/0 | 4258 | 2 | 0 | 1 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0052 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4234): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0061 | 0/0 | 4271 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4266): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0063 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4264): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0064 | 0/0 | 4267 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4262): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0068 | 0/0 | 4260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4255): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0069 | 0/0 | 4251 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4246): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0070 | 0/0 | 4257 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4252): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0071 | 0/0 | 4247 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4242): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0072 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4250): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0073 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4249): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0074 | 0/0 | 4253 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4248): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0075 | 0/0 | 4252 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4247): Show |
chr22 | 20854007 | 20896214 |
a0001c0002t0077 | 0/0 | 4253 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4248): Show |
chr22 | 20854007 | 20896214 |
a0001c0005t0028 | 0/0 | 4253 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4248): Show |
chr22 | 20854007 | 20896214 |
a0002c0003t0010 | 0/0 | 4258 | 7 | 0 | 3 | 4 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0002c0003t0018 | 0/0 | 4262 | 4 | 0 | 0 | 4 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4257): Show |
chr22 | 20854007 | 20896214 |
a0002c0003t0019 | 0/0 | 4260 | 4 | 0 | 0 | 4 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4255): Show |
chr22 | 20854007 | 20896214 |
a0002c0003t0080 | 0/0 | 4266 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4261): Show |
chr22 | 20854007 | 20896214 |
a0002c0003t0081 | 0/0 | 4264 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4259): Show |
chr22 | 20854007 | 20896214 |
a0003c0004t0001 | 0/0 | 4258 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4253): Show |
chr22 | 20854007 | 20896214 |
a0004c0006t0007 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | GTTCG others(4254): Show |
chr22 | 20854007 | 20896214 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0004 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0007g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0009g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0013g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0017g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0017g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0020g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0020g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0020g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0024g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0024g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0025g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0025g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0026g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0026g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0027g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0027g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0029g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0029g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0030g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0030g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0031g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0031g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0032g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0034g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0034g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0038g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0039g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0040g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0041g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0042g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0043g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0044g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0045g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0046g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0047g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0048g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0049g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0050g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0051g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0053g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0054g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0055g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0056g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0057g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0058g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0059g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0060g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0062g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0065g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0066g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0067g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0076g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0078g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0001t0079g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0008g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0011g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0011g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0011g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0012g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0012g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0012g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0012g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0012g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0014g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0014g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0014g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0015g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0015g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0015g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0015g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0016g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0016g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0016g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0021g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0021g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0021g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0022g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0022g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0023g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0023g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0023g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0033g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0033g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0035g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0035g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0036g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0036g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0037g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0037g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0052g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0061g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0063g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0064g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0068g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0069g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0070g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0071g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0072g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0073g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0074g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0075g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0002t0077g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0005t0028g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0001c0005t0028g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0010g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0010g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0010g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0010g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0010g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0018g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0018g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0018g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0018g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0019g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0019g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0019g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0019g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0080g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0002c0003t0081g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0003c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0003c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
a0004c0006t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0285 | EUR | GBR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0259 | EUR | FIN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00323 | hp2 | a0001 | c0002 | t0023 | g0228 | EUR | FIN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00423 | hp2 | a0002 | c0003 | t0018 | g0319 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00438 | hp1 | a0001 | c0002 | t0033 | g0277 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00558 | hp1 | a0001 | c0002 | t0004 | g0210 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00597 | hp1 | a0001 | c0002 | t0008 | g0292 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00609 | hp2 | a0002 | c0003 | t0019 | g0030 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00639 | hp2 | a0001 | c0002 | t0015 | g0263 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00642 | hp1 | a0001 | c0002 | t0005 | g0258 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00642 | hp2 | a0001 | c0002 | t0008 | g0027 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00673 | hp1 | a0001 | c0002 | t0016 | g0293 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | CHS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00738 | hp1 | a0001 | c0002 | t0071 | g0185 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0281 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0325 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01070 | hp1 | a0002 | c0003 | t0010 | g0250 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0305 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0326 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01071 | hp2 | a0002 | c0003 | t0010 | g0249 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01081 | hp2 | a0001 | c0002 | t0069 | g0314 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01106 | hp1 | a0001 | c0002 | t0015 | g0243 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01175 | hp1 | a0001 | c0001 | t0007 | g0324 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0298 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01255 | hp1 | a0001 | c0002 | t0037 | g0223 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01255 | hp2 | a0001 | c0002 | t0008 | g0272 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01256 | hp1 | a0001 | c0002 | t0036 | g0315 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01257 | hp2 | a0001 | c0002 | t0061 | g0271 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01261 | hp1 | a0001 | c0001 | t0017 | g0044 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01261 | hp2 | a0001 | c0002 | t0005 | g0260 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0262 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01358 | hp1 | a0001 | c0002 | t0005 | g0218 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01361 | hp2 | a0001 | c0002 | t0023 | g0217 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01515 | hp1 | a0001 | c0001 | t0025 | g0157 | EUR | IBS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0123 | EUR | IBS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01517 | hp2 | a0001 | c0001 | t0025 | g0158 | EUR | IBS | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01884 | hp1 | a0001 | c0005 | t0028 | g0206 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0197 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01934 | hp1 | a0001 | c0002 | t0008 | g0296 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0297 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01943 | hp2 | a0001 | c0001 | t0045 | g0095 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01952 | hp1 | a0001 | c0002 | t0016 | g0001 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0306 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0276 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01981 | hp2 | a0001 | c0002 | t0005 | g0261 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02015 | hp1 | a0001 | c0001 | t0009 | g0183 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02027 | hp1 | a0001 | c0002 | t0021 | g0294 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02055 | hp1 | a0001 | c0002 | t0022 | g0244 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02055 | hp2 | a0001 | c0001 | t0044 | g0054 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02056 | hp2 | a0002 | c0003 | t0010 | g0251 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02074 | hp2 | a0001 | c0002 | t0006 | g0012 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02083 | hp1 | a0001 | c0002 | t0008 | g0274 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02129 | hp1 | a0001 | c0002 | t0006 | g0001 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02145 | hp2 | a0001 | c0001 | t0066 | g0199 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0283 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | CDX | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02257 | hp1 | a0001 | c0001 | t0032 | g0023 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02257 | hp2 | a0001 | c0001 | t0013 | g0011 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02258 | hp2 | a0001 | c0001 | t0030 | g0252 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02273 | hp2 | a0001 | c0002 | t0008 | g0001 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02280 | hp1 | a0001 | c0001 | t0031 | g0011 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02572 | hp1 | a0001 | c0001 | t0029 | g0198 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0208 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02602 | hp2 | a0001 | c0002 | t0011 | g0232 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02615 | hp2 | a0001 | c0001 | t0034 | g0202 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02622 | hp1 | a0001 | c0001 | t0062 | g0192 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02622 | hp2 | a0001 | c0002 | t0011 | g0213 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02647 | hp1 | a0001 | c0001 | t0059 | g0025 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02647 | hp2 | a0001 | c0001 | t0076 | g0255 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02683 | hp2 | a0001 | c0002 | t0015 | g0221 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02738 | hp1 | a0001 | c0002 | t0012 | g0247 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02809 | hp2 | a0001 | c0002 | t0073 | g0024 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02818 | hp1 | a0001 | c0002 | t0005 | g0257 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02818 | hp2 | a0001 | c0001 | t0051 | g0034 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02886 | hp1 | a0001 | c0001 | t0055 | g0025 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02922 | hp1 | a0001 | c0002 | t0022 | g0266 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02922 | hp2 | a0001 | c0001 | t0032 | g0023 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02965 | hp1 | a0001 | c0001 | t0039 | g0238 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0191 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02970 | hp1 | a0001 | c0001 | t0024 | g0160 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02970 | hp2 | a0001 | c0001 | t0053 | g0022 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03017 | hp1 | a0001 | c0002 | t0012 | g0233 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0287 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0239 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03041 | hp2 | a0001 | c0001 | t0034 | g0203 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0214 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03098 | hp2 | a0001 | c0001 | t0079 | g0045 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03130 | hp2 | a0001 | c0001 | t0078 | g0264 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03195 | hp1 | a0004 | c0006 | t0007 | g0050 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03195 | hp2 | a0001 | c0001 | t0058 | g0031 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03209 | hp1 | a0001 | c0002 | t0004 | g0225 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03225 | hp1 | a0001 | c0002 | t0011 | g0209 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0112 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0310 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03453 | hp2 | a0001 | c0001 | t0067 | g0200 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03486 | hp1 | a0001 | c0001 | t0017 | g0049 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03486 | hp2 | a0001 | c0001 | t0060 | g0193 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03491 | hp1 | a0001 | c0002 | t0023 | g0313 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03491 | hp2 | a0001 | c0001 | t0026 | g0179 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03492 | hp2 | a0001 | c0001 | t0026 | g0181 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03540 | hp1 | a0001 | c0001 | t0031 | g0195 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | GWD | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03579 | hp1 | a0001 | c0002 | t0074 | g0323 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03579 | hp2 | a0001 | c0001 | t0030 | g0253 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0226 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0290 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03669 | hp1 | a0001 | c0002 | t0011 | g0236 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03704 | hp1 | a0001 | c0002 | t0004 | g0230 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03834 | hp1 | a0001 | c0002 | t0012 | g0231 | SAS | BEB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03927 | hp1 | a0001 | c0002 | t0004 | g0246 | SAS | BEB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | BEB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04115 | hp1 | a0001 | c0002 | t0037 | g0237 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04115 | hp2 | a0001 | c0002 | t0011 | g0235 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04184 | hp1 | a0001 | c0002 | t0036 | g0220 | SAS | BEB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04199 | hp1 | a0001 | c0001 | t0040 | g0151 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04199 | hp2 | a0001 | c0001 | t0050 | g0172 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04204 | hp2 | a0001 | c0002 | t0064 | g0270 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04228 | hp1 | a0001 | c0001 | t0046 | g0059 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | YRI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | YRI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18747 | hp1 | a0002 | c0003 | t0018 | g0013 | EAS | CHB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18747 | hp2 | a0001 | c0001 | t0009 | g0182 | EAS | CHB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18906 | hp1 | a0001 | c0001 | t0029 | g0194 | AFR | YRI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | YRI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18941 | hp1 | a0001 | c0001 | t0020 | g0162 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18941 | hp2 | a0001 | c0002 | t0068 | g0307 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18942 | hp1 | a0001 | c0002 | t0016 | g0002 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18943 | hp1 | a0001 | c0002 | t0008 | g0012 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18943 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18949 | hp2 | a0001 | c0001 | t0024 | g0148 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18950 | hp1 | a0001 | c0001 | t0027 | g0016 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18950 | hp2 | a0001 | c0002 | t0008 | g0300 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18952 | hp1 | a0001 | c0001 | t0038 | g0091 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18952 | hp2 | a0001 | c0001 | t0042 | g0147 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18959 | hp1 | a0001 | c0002 | t0014 | g0242 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0240 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18966 | hp2 | a0002 | c0003 | t0010 | g0254 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18967 | hp2 | a0001 | c0002 | t0005 | g0267 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18969 | hp2 | a0001 | c0002 | t0006 | g0288 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18972 | hp2 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18973 | hp2 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18974 | hp2 | a0001 | c0002 | t0021 | g0279 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18975 | hp2 | a0001 | c0002 | t0006 | g0311 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18977 | hp2 | a0001 | c0001 | t0047 | g0163 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18979 | hp2 | a0001 | c0002 | t0014 | g0245 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18985 | hp2 | a0002 | c0003 | t0080 | g0321 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18986 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18990 | hp2 | a0001 | c0002 | t0006 | g0269 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18992 | hp2 | a0002 | c0003 | t0010 | g0013 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18994 | hp1 | a0001 | c0002 | t0075 | g0186 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18994 | hp2 | a0002 | c0003 | t0019 | g0316 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18997 | hp2 | a0001 | c0002 | t0035 | g0275 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18999 | hp2 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19000 | hp1 | a0001 | c0002 | t0015 | g0268 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19000 | hp2 | a0002 | c0003 | t0018 | g0317 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19001 | hp1 | a0001 | c0001 | t0020 | g0066 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19001 | hp2 | a0001 | c0002 | t0016 | g0026 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19003 | hp1 | a0002 | c0003 | t0081 | g0030 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19003 | hp2 | a0001 | c0002 | t0014 | g0205 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19004 | hp2 | a0001 | c0002 | t0012 | g0224 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19005 | hp1 | a0001 | c0002 | t0033 | g0278 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19007 | hp1 | a0001 | c0001 | t0041 | g0134 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19007 | hp2 | a0001 | c0002 | t0070 | g0002 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19009 | hp1 | a0002 | c0003 | t0019 | g0320 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19009 | hp2 | a0001 | c0002 | t0005 | g0219 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19010 | hp1 | a0001 | c0002 | t0004 | g0204 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19030 | hp1 | a0001 | c0001 | t0054 | g0022 | AFR | LWK | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19030 | hp2 | a0001 | c0001 | t0056 | g0312 | AFR | LWK | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0011 | AFR | LWK | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19054 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19057 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19057 | hp2 | a0001 | c0002 | t0006 | g0302 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19060 | hp2 | a0002 | c0003 | t0019 | g0318 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19064 | hp2 | a0001 | c0002 | t0006 | g0309 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19065 | hp1 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19066 | hp2 | a0002 | c0003 | t0018 | g0322 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19068 | hp2 | a0001 | c0002 | t0063 | g0002 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19070 | hp2 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19072 | hp1 | a0001 | c0002 | t0052 | g0211 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19072 | hp2 | a0001 | c0001 | t0020 | g0065 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19077 | hp1 | a0001 | c0001 | t0048 | g0008 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19080 | hp1 | a0001 | c0002 | t0014 | g0234 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19083 | hp1 | a0001 | c0002 | t0035 | g0029 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19083 | hp2 | a0001 | c0001 | t0027 | g0074 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19085 | hp1 | a0001 | c0002 | t0021 | g0304 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19088 | hp2 | a0002 | c0003 | t0010 | g0013 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19240 | hp1 | a0001 | c0001 | t0057 | g0196 | AFR | YRI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA19240 | hp2 | a0001 | c0001 | t0065 | g0201 | AFR | YRI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0303 | EUR | TSI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0229 | SAS | GIH | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG01123 | hp2 | a0002 | c0003 | t0010 | g0248 | AMR | CLM | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02109 | hp2 | a0001 | c0001 | t0049 | g0187 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0256 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0184 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02559 | hp1 | a0001 | c0005 | t0028 | g0207 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG02559 | hp2 | a0003 | c0004 | t0001 | g0115 | AFR | ACB | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03471 | hp1 | a0001 | c0002 | t0022 | g0222 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | USA | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA18955 | hp2 | a0001 | c0002 | t0006 | g0190 | EAS | JPT | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA21309 | hp1 | a0001 | c0002 | t0077 | g0212 | AFR | LWK | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
NA21309 | hp2 | a0001 | c0002 | t0072 | g0215 | AFR | LWK | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
homoSapiens | chm13v2 | a0001 | c0002 | t0012 | g0227 | REF | REF | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
homoSapiens | grch38p0 | a0001 | c0001 | t0043 | g0002 | REF | REF | SNAP29_chr22_20854007_20896214 | SNAP29 | chr22 | 20854007 | 20896214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20859223 | C | T | 1 | a0004 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.113C>T | p.Pro38Leu | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 217/4259 | 113/777 | 38/258 | chr22 | 20859223 | |||
chr22:20859240 | T | C | 1 | a0003 | 2 | HG02559.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.130T>C | p.Tyr44His | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 234/4259 | 130/777 | 44/258 | chr22 | 20859240 | |||
chr22:20881101 | A | G | 1 | a0002 | 17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
missense_variant | MODERATE | c.487A>G | p.Ser163Gly | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/5 | 591/4259 | 487/777 | 163/258 | chr22 | 20881101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20859128 | A | G | 2 | a0001c0002 a0001c0005 |
136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
synonymous_variant | LOW | c.18A>G | p.Lys6Lys | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 122/4259 | 18/777 | 6/258 | chr22 | 20859128 | |||
chr22:20859182 | T | A | 1 | a0001c0005 | 2 | HG01884.hp1 HG02559.hp1 |
synonymous_variant | LOW | c.72T>A | p.Pro24Pro | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 176/4259 | 72/777 | 24/258 | chr22 | 20859182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20859043 | A | T | 5 | a0002c0003t0010 a0002c0003t0018 a0002c0003t0019 others(2): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-68A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 68 | chr22 | 20859043 | ||||||
chr22:20859057 | G | T | 2 | a0001c0001t0017 a0001c0001t0079 |
5 | HG01261.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | chr22 | 20859057 | |||||||
chr22:20859079 | C | G | 1 | a0001c0001t0078 | 1 | HG03130.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | chr22 | 20859079 | |||||||
chr22:20859092 | C | T | 51 | a0001c0001t0013 a0001c0001t0029 a0001c0001t0030 others(48): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-19C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | chr22 | 20859092 | |||||||
chr22:20859103 | C | G | 1 | a0001c0001t0051 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 8 | chr22 | 20859103 | ||||||
chr22:20859106 | G | A | 1 | a0001c0001t0051 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-5G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/5 | 5 | chr22 | 20859106 | ||||||
chr22:20887842 | G | A | 1 | a0001c0005t0028 | 2 | HG01884.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 6 | chr22 | 20887842 | ||||||
chr22:20887881 | A | G | 1 | a0001c0002t0077 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 45 | chr22 | 20887881 | ||||||
chr22:20887951 | TTATAATA others(12): Show |
T | 1 | a0001c0002t0052 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116_*134delTATAAT others(13): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 116 | chr22 | 20887951 | ||||||
chr22:20887959 | G | C | 6 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0025 others(3): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*123G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 123 | chr22 | 20887959 | ||||||
chr22:20887974 | C | T | 1 | a0001c0001t0050 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 138 | chr22 | 20887974 | ||||||
chr22:20888100 | G | A | 1 | a0001c0001t0038 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*264G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 264 | chr22 | 20888100 | ||||||
chr22:20888256 | A | G | 22 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0017 others(19): Show |
176 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 420 | chr22 | 20888256 | ||||||
chr22:20888311 | T | TCA | 5 | a0001c0001t0045 a0001c0001t0067 a0001c0002t0008 others(2): Show |
16 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*519_*520dupAC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACA | 4 | a0001c0001t0065 a0001c0001t0066 a0001c0002t0021 others(1): Show |
9 | HG00423.hp2 HG02027.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*520dupACAC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACA | 2 | a0001c0001t0032 a0002c0003t0081 |
3 | HG02257.hp1 HG02922.hp2 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*515_*520dupACACAC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(1): Show |
3 | a0001c0001t0039 a0001c0002t0064 a0002c0003t0080 |
3 | HG02965.hp1 HG04204.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*513_*520dupACACAC others(2): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(3): Show |
1 | a0001c0002t0063 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511_*520dupACACAC others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(5): Show |
4 | a0001c0001t0059 a0001c0001t0060 a0001c0001t0062 others(1): Show |
4 | HG01257.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*509_*520dupACACAC others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(7): Show |
2 | a0001c0001t0030 a0001c0001t0031 |
4 | HG02258.hp2 HG02280.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*507_*520dupACACAC others(8): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(9): Show |
1 | a0001c0001t0013 | 4 | HG01891.hp1 HG02257.hp2 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*505_*520dupACACAC others(10): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(11): Show |
3 | a0001c0001t0056 a0001c0001t0057 a0001c0001t0058 |
3 | HG03195.hp2 NA19030.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*503_*520dupACACAC others(12): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(13): Show |
2 | a0001c0001t0029 a0001c0001t0055 |
3 | HG02572.hp1 HG02886.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*501_*520dupACACAC others(14): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(15): Show |
1 | a0001c0001t0054 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*499_*520dupACACAC others(16): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | T | TCACACAC others(23): Show |
1 | a0001c0001t0053 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491_*520dupACACAC others(24): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | TCA | T | 7 | a0001c0002t0006 a0001c0002t0014 a0001c0002t0015 others(4): Show |
23 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*519_*520delAC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 519 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | TCACA | T | 7 | a0001c0002t0004 a0001c0002t0005 a0001c0002t0016 others(4): Show |
34 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*520delACAC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 517 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | TCACACA | T | 4 | a0001c0002t0011 a0001c0002t0074 a0001c0002t0077 others(1): Show |
9 | HG01884.hp1 HG02559.hp1 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*515_*520delACACAC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 515 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888311 | TCACACAC others(1): Show |
T | 2 | a0001c0002t0012 a0001c0002t0075 |
5 | HG02738.hp1 HG03017.hp1 HG03834.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*513_*520delACACAC others(2): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 513 | INFO_REALIGN_3_PRIME | chr22 | 20888311 | |||||
chr22:20888339 | ACACACAC others(11): Show |
A | 2 | a0001c0001t0009 a0001c0001t0044 |
8 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*505_*522delACACAC others(12): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 505 | INFO_REALIGN_3_PRIME | chr22 | 20888339 | |||||
chr22:20888341 | ACACACAC others(9): Show |
A | 1 | a0001c0001t0026 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*507_*522delACACAC others(10): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 507 | INFO_REALIGN_3_PRIME | chr22 | 20888341 | |||||
chr22:20888343 | ACACACAC others(7): Show |
A | 1 | a0001c0001t0049 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*509_*522delACACAC others(8): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 509 | INFO_REALIGN_3_PRIME | chr22 | 20888343 | |||||
chr22:20888345 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0024 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511_*522delACACAC others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 511 | INFO_REALIGN_3_PRIME | chr22 | 20888345 | |||||
chr22:20888347 | ACACACAC others(3): Show |
A | 4 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(1): Show |
7 | HG00733.hp2 HG01243.hp2 HG01346.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*513_*522delACACAC others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 513 | INFO_REALIGN_3_PRIME | chr22 | 20888347 | |||||
chr22:20888349 | ACACACAC others(1): Show |
A | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(17): Show |
151 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*515_*522delACACAC others(2): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 515 | INFO_REALIGN_3_PRIME | chr22 | 20888349 | |||||
chr22:20888351 | ACACACT | A | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0078 others(2): Show |
22 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*522delACACTC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 517 | INFO_REALIGN_3_PRIME | chr22 | 20888351 | |||||
chr22:20888353 | ACACT | A | 3 | a0001c0001t0001 a0002c0003t0010 a0003c0004t0001 |
11 | HG00423.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*519_*522delACTC | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 519 | INFO_REALIGN_3_PRIME | chr22 | 20888353 | |||||
chr22:20888355 | ACT | A | 4 | a0001c0001t0001 a0001c0001t0051 a0001c0001t0076 others(1): Show |
8 | HG01884.hp2 HG01952.hp2 HG02056.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*524_*525delCT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 524 | INFO_REALIGN_3_PRIME | chr22 | 20888355 | |||||
chr22:20888357 | T | A | 24 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0029 others(21): Show |
37 | HG00423.hp2 HG00609.hp2 HG01891.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*521T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 521 | chr22 | 20888357 | ||||||
chr22:20888563 | C | T | 1 | a0001c0001t0058 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 727 | chr22 | 20888563 | ||||||
chr22:20888576 | C | T | 3 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0044 |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*740C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 740 | chr22 | 20888576 | ||||||
chr22:20888591 | A | G | 2 | a0001c0002t0036 a0001c0002t0069 |
3 | HG01081.hp2 HG01256.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*755A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 755 | chr22 | 20888591 | ||||||
chr22:20888720 | C | A | 1 | a0001c0002t0070 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*884C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 884 | chr22 | 20888720 | ||||||
chr22:20888965 | T | C | 22 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0017 others(19): Show |
176 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1129T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1129 | chr22 | 20888965 | ||||||
chr22:20889021 | G | T | 1 | a0001c0001t0062 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1185 | chr22 | 20889021 | ||||||
chr22:20889235 | A | G | 1 | a0001c0001t0057 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1399A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1399 | chr22 | 20889235 | ||||||
chr22:20889322 | C | T | 1 | a0001c0002t0074 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1486C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1486 | chr22 | 20889322 | ||||||
chr22:20889326 | T | C | 17 | a0001c0001t0013 a0001c0001t0029 a0001c0001t0030 others(14): Show |
24 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1490T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1490 | chr22 | 20889326 | ||||||
chr22:20889355 | T | C | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0017 others(13): Show |
158 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1519T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1519 | chr22 | 20889355 | ||||||
chr22:20889399 | T | G | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(28): Show |
217 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1563T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1563 | chr22 | 20889399 | ||||||
chr22:20889425 | T | C | 1 | a0001c0002t0071 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1589T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1589 | chr22 | 20889425 | ||||||
chr22:20889563 | C | G | 1 | a0001c0001t0076 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1727C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 1727 | chr22 | 20889563 | ||||||
chr22:20889895 | C | T | 1 | a0001c0001t0048 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2059C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2059 | chr22 | 20889895 | ||||||
chr22:20889941 | T | C | 1 | a0001c0002t0072 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2105T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2105 | chr22 | 20889941 | ||||||
chr22:20889941 | T | G | 6 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0025 others(3): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2105T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2105 | chr22 | 20889941 | ||||||
chr22:20889947 | G | T | 1 | a0001c0002t0068 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2111 | chr22 | 20889947 | ||||||
chr22:20889957 | T | C | 1 | a0001c0001t0049 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2121T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2121 | chr22 | 20889957 | ||||||
chr22:20890096 | C | T | 1 | a0001c0001t0049 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2260C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2260 | chr22 | 20890096 | ||||||
chr22:20890097 | G | T | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0017 others(13): Show |
158 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2261G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2261 | chr22 | 20890097 | ||||||
chr22:20890113 | C | T | 1 | a0001c0001t0078 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2277C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2277 | chr22 | 20890113 | ||||||
chr22:20890116 | G | A | 1 | a0001c0002t0035 | 2 | NA18997.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2280G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2280 | chr22 | 20890116 | ||||||
chr22:20890243 | C | G | 1 | a0001c0001t0047 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2407C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2407 | chr22 | 20890243 | ||||||
chr22:20890387 | G | A | 1 | a0001c0002t0023 | 3 | HG00323.hp2 HG01361.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2551G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2551 | chr22 | 20890387 | ||||||
chr22:20890424 | T | C | 1 | a0001c0001t0040 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2588 | chr22 | 20890424 | ||||||
chr22:20890459 | C | T | 1 | a0001c0001t0056 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2623C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2623 | chr22 | 20890459 | ||||||
chr22:20890528 | C | T | 5 | a0002c0003t0010 a0002c0003t0018 a0002c0003t0019 others(2): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2692C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2692 | chr22 | 20890528 | ||||||
chr22:20890619 | C | T | 1 | a0001c0001t0025 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2783C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2783 | chr22 | 20890619 | ||||||
chr22:20890627 | T | C | 1 | a0001c0001t0025 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2791T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2791 | chr22 | 20890627 | ||||||
chr22:20890631 | C | T | 12 | a0001c0001t0013 a0001c0001t0029 a0001c0001t0031 others(9): Show |
18 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2795C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2795 | chr22 | 20890631 | ||||||
chr22:20890632 | G | A | 1 | a0001c0001t0046 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2796G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2796 | chr22 | 20890632 | ||||||
chr22:20890652 | A | G | 70 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(67): Show |
305 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2816A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2816 | chr22 | 20890652 | ||||||
chr22:20890692 | G | A | 17 | a0001c0001t0013 a0001c0001t0029 a0001c0001t0030 others(14): Show |
24 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2856G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2856 | chr22 | 20890692 | ||||||
chr22:20890708 | G | A | 1 | a0001c0001t0051 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2872 | chr22 | 20890708 | ||||||
chr22:20890715 | C | T | 5 | a0002c0003t0010 a0002c0003t0018 a0002c0003t0019 others(2): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2879C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2879 | chr22 | 20890715 | ||||||
chr22:20890728 | C | T | 1 | a0001c0001t0078 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2892C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2892 | chr22 | 20890728 | ||||||
chr22:20890758 | C | CA | 6 | a0001c0001t0027 a0001c0001t0034 a0001c0002t0033 others(3): Show |
9 | HG00438.hp1 HG02615.hp2 HG03041.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2944dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2945 | INFO_REALIGN_3_PRIME | chr22 | 20890758 | |||||
chr22:20890758 | CA | C | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(34): Show |
215 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2944delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2944 | INFO_REALIGN_3_PRIME | chr22 | 20890758 | |||||
chr22:20890758 | CAAA | C | 2 | a0001c0001t0009 a0001c0001t0026 |
9 | HG02015.hp1 HG02486.hp2 HG03491.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2942_*2944delAAA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2942 | INFO_REALIGN_3_PRIME | chr22 | 20890758 | |||||
chr22:20890758 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0041 a0001c0002t0005 a0001c0002t0015 others(4): Show |
23 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2937_*2944delAAAA others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2937 | INFO_REALIGN_3_PRIME | chr22 | 20890758 | |||||
chr22:20890797 | T | C | 22 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0017 others(19): Show |
176 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2961T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 2961 | chr22 | 20890797 | ||||||
chr22:20890851 | G | A | 3 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0044 |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3015G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 3015 | chr22 | 20890851 | ||||||
chr22:20890931 | C | T | 1 | a0001c0001t0049 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3095C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 3095 | chr22 | 20890931 | ||||||
chr22:20891000 | A | C | 1 | a0001c0001t0076 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3164A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 3164 | chr22 | 20891000 | ||||||
chr22:20891082 | A | G | 1 | a0001c0001t0020 | 3 | NA18941.hp1 NA19001.hp1 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3246A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 3246 | chr22 | 20891082 | ||||||
chr22:20891121 | G | T | 1 | a0001c0001t0058 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3285G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 5/5 | 3285 | chr22 | 20891121 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20859435 | A | T | 2 | a0001c0002t0002g0325 a0001c0002t0002g0326 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.237+88A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20859435 | |||||||
chr22:20859741 | A | G | 1 | a0001c0001t0007g0324 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.237+394A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20859741 | |||||||
chr22:20859749 | C | T | 1 | a0001c0002t0074g0323 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.237+402C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20859749 | |||||||
chr22:20860131 | G | A | 1 | a0001c0001t0058g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.237+784G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860131 | |||||||
chr22:20860156 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.237+809G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860156 | |||||||
chr22:20860194 | T | TA | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(151): Show |
174 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.237+862dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20860194 | ||||||
chr22:20860194 | T | TAA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(22): Show |
27 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.237+861_237+862dup others(2): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20860194 | ||||||
chr22:20860194 | TA | T | 14 | a0001c0002t0023g0313 a0001c0002t0036g0315 a0001c0002t0069g0314 others(11): Show |
15 | HG00423.hp2 HG00609.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.237+862delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20860194 | ||||||
chr22:20860371 | CT | C | 87 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0030g0252 others(84): Show |
88 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.237+1040delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20860371 | ||||||
chr22:20860371 | CTT | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
213 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.237+1039_237+1040d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20860371 | ||||||
chr22:20860527 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.237+1180C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860527 | |||||||
chr22:20860839 | G | T | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1492G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860839 | |||||||
chr22:20860840 | G | C | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1493G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860840 | |||||||
chr22:20860842 | G | T | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1495G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860842 | |||||||
chr22:20860845 | T | A | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1498T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860845 | |||||||
chr22:20860846 | GAGACCAG others(66): Show |
G | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1500_237+1572d others(75): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860846 | |||||||
chr22:20860910 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
197 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.237+1563A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860910 | |||||||
chr22:20860924 | C | A | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1577C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860924 | |||||||
chr22:20860926 | A | C | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1579A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860926 | |||||||
chr22:20860927 | C | A | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1580C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860927 | |||||||
chr22:20860929 | G | T | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1582G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860929 | |||||||
chr22:20860930 | A | G | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1583A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860930 | |||||||
chr22:20860931 | G | T | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1584G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860931 | |||||||
chr22:20860932 | G | A | 2 | a0001c0001t0058g0031 a0001c0001t0078g0264 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.237+1585G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20860932 | |||||||
chr22:20861067 | C | G | 8 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(5): Show |
8 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+1720C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861067 | |||||||
chr22:20861075 | C | T | 1 | a0001c0001t0065g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.237+1728C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861075 | |||||||
chr22:20861117 | G | GT | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+1770_237+1771i others(3): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861117 | |||||||
chr22:20861118 | G | GT | 64 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(61): Show |
69 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.237+1789dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20861118 | ||||||
chr22:20861118 | G | GTT | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(124): Show |
146 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.237+1788_237+1789d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20861118 | ||||||
chr22:20861118 | G | GTTT | 20 | a0001c0001t0001g0052 a0001c0001t0001g0161 a0001c0001t0001g0164 others(17): Show |
20 | HG01081.hp1 HG01175.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.237+1787_237+1789d others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20861118 | ||||||
chr22:20861118 | G | T | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+1771G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861118 | |||||||
chr22:20861413 | C | T | 1 | a0001c0001t0009g0184 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.237+2066C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861413 | |||||||
chr22:20861454 | T | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(113): Show |
134 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.237+2107T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861454 | |||||||
chr22:20861481 | A | G | 3 | a0001c0002t0004g0240 a0001c0002t0004g0241 a0001c0002t0014g0242 |
3 | NA18959.hp1 NA18964.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.237+2134A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861481 | |||||||
chr22:20861482 | G | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
198 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.237+2135G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861482 | |||||||
chr22:20861700 | A | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(17): Show |
22 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.237+2353A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861700 | |||||||
chr22:20861784 | G | A | 2 | a0001c0001t0034g0202 a0001c0001t0034g0203 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.237+2437G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861784 | |||||||
chr22:20861826 | G | A | 1 | a0001c0002t0002g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.237+2479G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861826 | |||||||
chr22:20861912 | C | T | 1 | a0001c0002t0006g0309 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.237+2565C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861912 | |||||||
chr22:20861994 | G | A | 2 | a0001c0002t0004g0204 a0001c0002t0014g0205 |
2 | NA19003.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.237+2647G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861994 | |||||||
chr22:20861994 | G | T | 1 | a0001c0002t0004g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.237+2647G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20861994 | |||||||
chr22:20862057 | A | C | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+2710A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862057 | |||||||
chr22:20862270 | A | T | 4 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0055g0025 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+2923A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862270 | |||||||
chr22:20862296 | T | G | 2 | a0001c0005t0028g0206 a0001c0005t0028g0207 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.237+2949T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862296 | |||||||
chr22:20862407 | A | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(215): Show |
243 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.237+3060A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862407 | |||||||
chr22:20862551 | G | A | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+3204G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862551 | |||||||
chr22:20862610 | G | C | 1 | a0001c0001t0078g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.237+3263G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862610 | |||||||
chr22:20862624 | G | T | 1 | a0001c0002t0012g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.237+3277G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862624 | |||||||
chr22:20862636 | C | T | 11 | a0001c0002t0004g0204 a0001c0002t0004g0229 a0001c0002t0004g0230 others(8): Show |
11 | HG02602.hp2 HG03017.hp1 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.237+3289C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862636 | |||||||
chr22:20862812 | A | G | 1 | a0001c0001t0067g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237+3465A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862812 | |||||||
chr22:20862893 | G | A | 1 | a0001c0002t0004g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.237+3546G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862893 | |||||||
chr22:20862944 | C | T | 2 | a0001c0001t0034g0202 a0001c0001t0034g0203 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.237+3597C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20862944 | |||||||
chr22:20863217 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0161 |
2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.237+3870G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20863217 | |||||||
chr22:20863287 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
218 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.237+3940A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20863287 | |||||||
chr22:20863314 | G | GCCT | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.237+3968_237+3970d others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20863314 | ||||||
chr22:20863598 | G | A | 1 | a0001c0002t0011g0209 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.237+4251G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20863598 | |||||||
chr22:20863898 | T | G | 1 | a0001c0001t0046g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.237+4551T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20863898 | |||||||
chr22:20863936 | A | C | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.237+4589A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20863936 | |||||||
chr22:20863952 | T | G | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+4605T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20863952 | |||||||
chr22:20864051 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
133 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.237+4704A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864051 | |||||||
chr22:20864303 | C | T | 1 | a0001c0002t0023g0228 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.237+4956C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864303 | |||||||
chr22:20864449 | A | G | 1 | a0001c0002t0002g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.237+5102A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864449 | |||||||
chr22:20864468 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG01891.hp2 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.237+5121A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864468 | |||||||
chr22:20864588 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
218 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.237+5241A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864588 | |||||||
chr22:20864589 | C | T | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.237+5242C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864589 | |||||||
chr22:20864985 | T | C | 2 | a0001c0002t0004g0210 a0001c0002t0052g0211 |
2 | HG00558.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.238-5352T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20864985 | |||||||
chr22:20865001 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.238-5336C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865001 | |||||||
chr22:20865142 | C | T | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-5195C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865142 | |||||||
chr22:20865213 | G | A | 7 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0011g0209 others(4): Show |
7 | HG02622.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-5124G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865213 | |||||||
chr22:20865283 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-5054A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865283 | |||||||
chr22:20865284 | G | A | 1 | a0001c0002t0022g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.238-5053G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865284 | |||||||
chr22:20865355 | A | C | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.238-4982A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865355 | |||||||
chr22:20865407 | G | A | 2 | a0001c0001t0034g0202 a0001c0001t0034g0203 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.238-4930G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865407 | |||||||
chr22:20865422 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0007g0123 |
3 | HG01106.hp2 HG01192.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.238-4915C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865422 | |||||||
chr22:20865430 | G | A | 3 | a0002c0003t0010g0248 a0002c0003t0010g0249 a0002c0003t0010g0250 |
3 | HG01070.hp1 HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.238-4907G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865430 | |||||||
chr22:20865656 | C | T | 2 | a0001c0005t0028g0206 a0001c0005t0028g0207 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.238-4681C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865656 | |||||||
chr22:20865716 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-4621T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865716 | |||||||
chr22:20865717 | G | A | 2 | a0001c0001t0003g0133 a0001c0001t0041g0134 |
2 | HG02071.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.238-4620G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865717 | |||||||
chr22:20865941 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
156 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.238-4396A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865941 | |||||||
chr22:20865942 | C | G | 1 | a0001c0001t0007g0057 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.238-4395C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20865942 | |||||||
chr22:20866043 | G | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(262): Show |
290 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.238-4294G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866043 | |||||||
chr22:20866297 | C | T | 1 | a0002c0003t0010g0251 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.238-4040C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866297 | |||||||
chr22:20866363 | C | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
157 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.238-3974C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866363 | |||||||
chr22:20866381 | T | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-3956T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866381 | |||||||
chr22:20866418 | C | T | 1 | a0001c0001t0076g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238-3919C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866418 | |||||||
chr22:20866445 | C | T | 30 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(27): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.238-3892C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866445 | |||||||
chr22:20866466 | C | G | 1 | a0001c0002t0068g0307 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.238-3871C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866466 | |||||||
chr22:20866541 | G | A | 1 | a0001c0001t0076g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238-3796G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866541 | |||||||
chr22:20866643 | G | A | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238-3694G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866643 | |||||||
chr22:20866719 | C | T | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-3618C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866719 | |||||||
chr22:20866732 | C | T | 1 | a0001c0002t0002g0306 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.238-3605C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866732 | |||||||
chr22:20866751 | C | G | 1 | a0001c0002t0004g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.238-3586C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866751 | |||||||
chr22:20866962 | C | T | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238-3375C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20866962 | |||||||
chr22:20867016 | G | A | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-3321G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20867016 | |||||||
chr22:20867017 | A | G | 30 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(27): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.238-3320A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20867017 | |||||||
chr22:20867430 | T | C | 1 | a0001c0001t0076g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238-2907T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20867430 | |||||||
chr22:20867517 | A | G | 8 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(5): Show |
8 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-2820A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20867517 | |||||||
chr22:20867561 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-2776A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20867561 | |||||||
chr22:20867983 | G | A | 1 | a0001c0002t0006g0269 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.238-2354G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20867983 | |||||||
chr22:20868098 | C | T | 1 | a0001c0002t0022g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238-2239C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868098 | |||||||
chr22:20868099 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.238-2238G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868099 | |||||||
chr22:20868170 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-2167G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868170 | |||||||
chr22:20868171 | A | G | 1 | a0001c0001t0076g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238-2166A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868171 | |||||||
chr22:20868281 | TA | T | 7 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0011g0209 others(4): Show |
7 | HG02622.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-2050delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20868281 | ||||||
chr22:20868333 | T | A | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-2004T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868333 | |||||||
chr22:20868338 | G | A | 1 | a0002c0003t0019g0316 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.238-1999G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868338 | |||||||
chr22:20868496 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0024g0160 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.238-1841C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868496 | |||||||
chr22:20868615 | T | TA | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(135): Show |
158 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.238-1716dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 20868615 | ||||||
chr22:20868674 | T | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.238-1663T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20868674 | |||||||
chr22:20869004 | C | T | 16 | a0002c0003t0010g0013 a0002c0003t0010g0248 a0002c0003t0010g0249 others(13): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.238-1333C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869004 | |||||||
chr22:20869005 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.238-1332G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869005 | |||||||
chr22:20869015 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-1322G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869015 | |||||||
chr22:20869276 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-1061T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869276 | |||||||
chr22:20869295 | T | A | 2 | a0001c0002t0061g0271 a0001c0002t0064g0270 |
2 | HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.238-1042T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869295 | |||||||
chr22:20869302 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.238-1035A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869302 | |||||||
chr22:20869309 | T | A | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238-1028T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869309 | |||||||
chr22:20869464 | A | G | 1 | a0001c0002t0036g0315 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.238-873A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869464 | |||||||
chr22:20869735 | A | G | 3 | a0001c0001t0003g0156 a0001c0001t0025g0157 a0001c0001t0025g0158 |
3 | HG01433.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.238-602A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869735 | |||||||
chr22:20869789 | G | A | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-548G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869789 | |||||||
chr22:20869807 | G | A | 1 | a0001c0002t0008g0272 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.238-530G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869807 | |||||||
chr22:20869808 | T | A | 1 | a0001c0002t0002g0273 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.238-529T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869808 | |||||||
chr22:20869809 | C | T | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238-528C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869809 | |||||||
chr22:20869810 | G | A | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-527G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20869810 | |||||||
chr22:20870015 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01109.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.238-322C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20870015 | |||||||
chr22:20870016 | G | A | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238-321G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20870016 | |||||||
chr22:20870046 | G | A | 21 | a0001c0001t0013g0011 a0001c0001t0013g0191 a0001c0001t0013g0197 others(18): Show |
23 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.238-291G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20870046 | |||||||
chr22:20870293 | G | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02165.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-44G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 1/4 | chr22 | 20870293 | |||||||
chr22:20870612 | G | A | 16 | a0002c0003t0010g0013 a0002c0003t0010g0248 a0002c0003t0010g0249 others(13): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.434+79G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870612 | |||||||
chr22:20870737 | G | T | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.434+204G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870737 | |||||||
chr22:20870846 | A | T | 16 | a0002c0003t0010g0013 a0002c0003t0010g0248 a0002c0003t0010g0249 others(13): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.434+313A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870846 | |||||||
chr22:20870887 | G | A | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.434+354G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870887 | |||||||
chr22:20870982 | ACCCAGGC others(3): Show |
A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+450_434+459del others(10): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870982 | |||||||
chr22:20870993 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+460G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870993 | |||||||
chr22:20870994 | T | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+461T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870994 | |||||||
chr22:20870996 | G | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+463G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870996 | |||||||
chr22:20870998 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+465G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870998 | |||||||
chr22:20870999 | C | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+466C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20870999 | |||||||
chr22:20871002 | A | G | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+469A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871002 | |||||||
chr22:20871003 | C | G | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+470C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871003 | |||||||
chr22:20871005 | T | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+472T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871005 | |||||||
chr22:20871006 | G | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+473G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871006 | |||||||
chr22:20871021 | C | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+488C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871021 | |||||||
chr22:20871022 | A | G | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+489A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871022 | |||||||
chr22:20871024 | G | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+491G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871024 | |||||||
chr22:20871026 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+493G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871026 | |||||||
chr22:20871027 | G | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+494G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871027 | |||||||
chr22:20871028 | C | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+495C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871028 | |||||||
chr22:20871030 | G | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+497G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871030 | |||||||
chr22:20871033 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+500G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871033 | |||||||
chr22:20871035 | A | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+502A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871035 | |||||||
chr22:20871036 | A | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+503A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871036 | |||||||
chr22:20871037 | G | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+504G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871037 | |||||||
chr22:20871041 | A | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+508A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871041 | |||||||
chr22:20871047 | T | G | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+514T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871047 | |||||||
chr22:20871048 | G | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+515G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871048 | |||||||
chr22:20871051 | G | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+518G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871051 | |||||||
chr22:20871052 | C | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+519C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871052 | |||||||
chr22:20871053 | C | G | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+520C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871053 | |||||||
chr22:20871057 | A | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+524A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871057 | |||||||
chr22:20871058 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+525G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871058 | |||||||
chr22:20871059 | A | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+526A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871059 | |||||||
chr22:20871071 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+538G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871071 | |||||||
chr22:20871075 | G | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+542G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871075 | |||||||
chr22:20871076 | C | T | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+543C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871076 | |||||||
chr22:20871078 | G | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+545G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871078 | |||||||
chr22:20871080 | A | C | 1 | a0001c0001t0009g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.434+547A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871080 | |||||||
chr22:20871125 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.434+592G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871125 | |||||||
chr22:20871125 | GA | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
60 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.434+608delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871125 | ||||||
chr22:20871137 | A | T | 6 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0125 others(3): Show |
6 | HG00423.hp1 HG00741.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+604A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871137 | |||||||
chr22:20871138 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.434+605A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871138 | |||||||
chr22:20871148 | A | G | 1 | a0001c0002t0037g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.434+615A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871148 | |||||||
chr22:20871318 | TA | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0175 a0001c0001t0034g0203 others(3): Show |
6 | HG02976.hp1 HG03041.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+800delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871318 | ||||||
chr22:20871353 | C | T | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.434+820C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871353 | |||||||
chr22:20871460 | A | T | 2 | a0002c0003t0010g0249 a0002c0003t0010g0250 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.434+927A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871460 | |||||||
chr22:20871473 | C | G | 3 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0072g0215 |
3 | HG03041.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.434+940C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871473 | |||||||
chr22:20871482 | T | TA | 66 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0035 others(63): Show |
71 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.434+972dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | T | TAAAAAAA others(2): Show |
8 | a0001c0001t0003g0133 a0001c0001t0003g0152 a0001c0001t0003g0153 others(5): Show |
8 | HG01243.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+964_434+972dup others(9): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | T | TAAAAAAA others(3): Show |
14 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0143 others(11): Show |
15 | HG01074.hp1 HG01123.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.434+963_434+972dup others(10): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | T | TAAAAAAA others(4): Show |
6 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0003g0139 others(3): Show |
6 | HG00673.hp2 HG02027.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+962_434+972dup others(11): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0003g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.434+961_434+972dup others(12): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0003g0135 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.434+960_434+972dup others(13): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | T | TAAAAAAA others(65): Show |
1 | a0001c0001t0020g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.434+972_434+973ins others(72): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871482 | TA | T | 16 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0101 others(13): Show |
16 | HG00099.hp2 HG00280.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.434+972delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20871482 | ||||||
chr22:20871557 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.434+1024C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871557 | |||||||
chr22:20871637 | C | T | 1 | a0001c0001t0020g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.434+1104C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871637 | |||||||
chr22:20871654 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.434+1121G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871654 | |||||||
chr22:20871803 | A | C | 1 | a0004c0006t0007g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.434+1270A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871803 | |||||||
chr22:20871837 | A | G | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.434+1304A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871837 | |||||||
chr22:20871877 | G | A | 1 | a0001c0002t0004g0240 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.434+1344G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871877 | |||||||
chr22:20871902 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.434+1369G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20871902 | |||||||
chr22:20872055 | G | A | 1 | a0001c0002t0004g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.434+1522G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872055 | |||||||
chr22:20872216 | CTT | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.434+1686_434+1687d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872216 | ||||||
chr22:20872249 | A | AT | 28 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.434+1724dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872249 | ||||||
chr22:20872249 | A | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(17): Show |
22 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.434+1716A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872249 | |||||||
chr22:20872409 | C | CT | 16 | a0002c0003t0010g0013 a0002c0003t0010g0248 a0002c0003t0010g0249 others(13): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.434+1885dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872409 | ||||||
chr22:20872409 | CT | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.434+1885delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872409 | ||||||
chr22:20872412 | T | G | 7 | a0001c0001t0013g0191 a0001c0001t0029g0194 a0001c0001t0031g0195 others(4): Show |
7 | HG02622.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+1879T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872412 | |||||||
chr22:20872435 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.434+1902C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872435 | |||||||
chr22:20872469 | C | A | 16 | a0002c0003t0010g0013 a0002c0003t0010g0248 a0002c0003t0010g0249 others(13): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.434+1936C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872469 | |||||||
chr22:20872469 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.434+1936C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872469 | |||||||
chr22:20872505 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02129.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.434+1972G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872505 | |||||||
chr22:20872602 | G | A | 6 | a0001c0001t0001g0099 a0001c0002t0002g0005 a0001c0002t0002g0305 others(3): Show |
9 | HG01070.hp2 HG01975.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+2069G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872602 | |||||||
chr22:20872624 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
198 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.434+2091C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872624 | |||||||
chr22:20872647 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.434+2114G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872647 | |||||||
chr22:20872820 | C | CT | 65 | a0001c0001t0001g0175 a0001c0001t0003g0053 a0001c0001t0009g0021 others(62): Show |
67 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.434+2314dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872820 | ||||||
chr22:20872820 | C | CTT | 41 | a0001c0001t0003g0020 a0001c0001t0003g0136 a0001c0001t0003g0137 others(38): Show |
44 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.434+2313_434+2314d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872820 | ||||||
chr22:20872820 | C | CTTT | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0019 others(62): Show |
68 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.434+2312_434+2314d others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872820 | ||||||
chr22:20872820 | C | CTTTT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
66 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.434+2311_434+2314d others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872820 | ||||||
chr22:20872820 | C | CTTTTT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
48 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.434+2310_434+2314d others(7): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872820 | ||||||
chr22:20872820 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0055g0025 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+2303_434+2314d others(14): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20872820 | ||||||
chr22:20872905 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.434+2372C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20872905 | |||||||
chr22:20873066 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.434+2533A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20873066 | |||||||
chr22:20873695 | TG | T | 4 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0055g0025 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+3164delG | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20873695 | ||||||
chr22:20873707 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.434+3174C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20873707 | |||||||
chr22:20873793 | C | A | 1 | a0001c0001t0020g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.434+3260C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20873793 | |||||||
chr22:20873879 | A | C | 1 | a0001c0002t0014g0234 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.434+3346A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20873879 | |||||||
chr22:20873964 | C | CA | 65 | a0001c0001t0001g0169 a0001c0001t0020g0162 a0001c0002t0002g0001 others(62): Show |
70 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.434+3460dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20873964 | ||||||
chr22:20873964 | C | CAA | 29 | a0001c0002t0002g0289 a0001c0002t0004g0204 a0001c0002t0004g0229 others(26): Show |
29 | HG00423.hp2 HG00609.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.434+3459_434+3460d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20873964 | ||||||
chr22:20873964 | CA | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(71): Show |
83 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.434+3460delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20873964 | ||||||
chr22:20873964 | CAA | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(87): Show |
105 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.434+3459_434+3460d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20873964 | ||||||
chr22:20873964 | CAAA | C | 16 | a0001c0001t0001g0038 a0001c0001t0003g0137 a0001c0001t0003g0138 others(13): Show |
16 | HG00673.hp2 HG01123.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.434+3458_434+3460d others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20873964 | ||||||
chr22:20874213 | TACAGTGA others(20): Show |
T | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.434+3708_434+3734d others(29): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874213 | ||||||
chr22:20874287 | G | A | 3 | a0002c0003t0010g0248 a0002c0003t0010g0249 a0002c0003t0010g0250 |
3 | HG01070.hp1 HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.434+3754G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874287 | |||||||
chr22:20874296 | TGACACAC others(3): Show |
T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0079 a0001c0001t0001g0080 others(8): Show |
11 | HG01081.hp1 HG01358.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.434+3784_434+3793d others(12): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874296 | ||||||
chr22:20874307 | G | GAC | 12 | a0002c0003t0010g0013 a0002c0003t0010g0254 a0002c0003t0018g0013 others(9): Show |
13 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.434+3782_434+3783d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874307 | ||||||
chr22:20874313 | CACAG | C | 3 | a0002c0003t0010g0248 a0002c0003t0010g0249 a0002c0003t0010g0250 |
3 | HG01070.hp1 HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.434+3784_434+3787d others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874313 | ||||||
chr22:20874317 | G | C | 13 | a0002c0003t0010g0013 a0002c0003t0010g0251 a0002c0003t0010g0254 others(10): Show |
14 | HG00423.hp2 HG00609.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.434+3784G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874317 | |||||||
chr22:20874317 | G | GAC | 34 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(31): Show |
36 | HG00438.hp1 HG01109.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.434+3805_434+3806d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874317 | ||||||
chr22:20874317 | G | GACAC | 36 | a0001c0001t0001g0037 a0001c0001t0003g0020 a0001c0001t0003g0053 others(33): Show |
38 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.434+3803_434+3806d others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874317 | ||||||
chr22:20874317 | GACACACA others(26): Show |
G | 1 | a0001c0002t0061g0271 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.434+3807_434+3839d others(35): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874317 | ||||||
chr22:20874318 | ACACACAC others(24): Show |
A | 1 | a0001c0002t0064g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.434+3807_434+3837d others(33): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874318 | ||||||
chr22:20874327 | C | G | 2 | a0001c0001t0034g0202 a0001c0001t0034g0203 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.434+3794C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874327 | |||||||
chr22:20874349 | CCACA | C | 7 | a0001c0001t0051g0034 a0001c0002t0002g0002 a0001c0002t0002g0026 others(4): Show |
7 | HG00280.hp1 HG00738.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+3860_434+3863d others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACA | C | 42 | a0001c0002t0002g0001 a0001c0002t0002g0027 a0001c0002t0002g0284 others(39): Show |
42 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.434+3858_434+3863d others(8): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(1): Show |
C | 60 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0038 others(57): Show |
65 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.434+3856_434+3863d others(10): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(3): Show |
C | 29 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0037 others(26): Show |
29 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.434+3854_434+3863d others(12): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(5): Show |
C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(39): Show |
47 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.434+3852_434+3863d others(14): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(7): Show |
C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(120): Show |
138 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.434+3850_434+3863d others(16): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(9): Show |
C | 3 | a0001c0001t0001g0055 a0001c0002t0002g0001 a0001c0002t0002g0282 |
3 | HG04228.hp2 NA18965.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.434+3848_434+3863d others(18): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(11): Show |
C | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.434+3846_434+3863d others(20): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(13): Show |
C | 4 | a0001c0001t0003g0156 a0001c0001t0025g0157 a0001c0001t0025g0158 others(1): Show |
4 | HG01433.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+3844_434+3863d others(22): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(15): Show |
C | 29 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(26): Show |
30 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.434+3842_434+3863d others(24): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874349 | CCACACAC others(17): Show |
C | 3 | a0001c0001t0020g0065 a0001c0001t0020g0066 a0001c0001t0047g0163 |
3 | NA18977.hp2 NA19001.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.434+3840_434+3863d others(26): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874349 | ||||||
chr22:20874350 | CACACA | C | 6 | a0001c0002t0004g0229 a0001c0002t0004g0246 a0001c0002t0005g0258 others(3): Show |
6 | HG00642.hp1 HG03669.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+3818_434+3822d others(7): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874350 | |||||||
chr22:20874352 | CACACACA others(16): Show |
C | 1 | a0001c0001t0020g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.434+3820_434+3842d others(25): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874352 | |||||||
chr22:20874355 | A | C | 2 | a0001c0002t0005g0260 a0001c0002t0011g0235 |
2 | HG01261.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.434+3822A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874355 | |||||||
chr22:20874357 | A | C | 26 | a0001c0002t0004g0204 a0001c0002t0004g0230 a0001c0002t0005g0216 others(23): Show |
26 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.434+3824A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874357 | |||||||
chr22:20874359 | A | C | 6 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0011g0209 others(3): Show |
6 | HG03017.hp1 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+3826A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874359 | |||||||
chr22:20874361 | A | C | 2 | a0001c0005t0028g0206 a0001c0005t0028g0207 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.434+3828A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874361 | |||||||
chr22:20874411 | C | T | 1 | a0001c0002t0021g0304 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.434+3878C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874411 | |||||||
chr22:20874536 | G | A | 1 | a0001c0001t0078g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.434+4003G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874536 | |||||||
chr22:20874574 | C | CA | 58 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0089 others(55): Show |
60 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.434+4060dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874574 | ||||||
chr22:20874574 | CAA | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0047 others(7): Show |
11 | HG01261.hp1 HG02647.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.434+4059_434+4060d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20874574 | ||||||
chr22:20874624 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.434+4091C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874624 | |||||||
chr22:20874646 | G | C | 1 | a0001c0002t0022g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.434+4113G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874646 | |||||||
chr22:20874754 | C | T | 18 | a0001c0001t0039g0238 a0001c0001t0049g0187 a0002c0003t0010g0013 others(15): Show |
19 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.434+4221C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874754 | |||||||
chr22:20874795 | G | T | 4 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0055g0025 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+4262G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20874795 | |||||||
chr22:20875079 | T | A | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.434+4546T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875079 | |||||||
chr22:20875276 | C | T | 30 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(27): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.434+4743C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875276 | |||||||
chr22:20875296 | T | G | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.434+4763T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875296 | |||||||
chr22:20875376 | A | C | 18 | a0001c0001t0039g0238 a0001c0001t0049g0187 a0002c0003t0010g0013 others(15): Show |
19 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.434+4843A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875376 | |||||||
chr22:20875425 | A | T | 1 | a0001c0002t0008g0296 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.434+4892A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875425 | |||||||
chr22:20875449 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(17): Show |
22 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.434+4916T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875449 | |||||||
chr22:20875465 | T | G | 1 | a0001c0002t0004g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.434+4932T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875465 | |||||||
chr22:20875514 | A | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(44): Show |
49 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.434+4981A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875514 | |||||||
chr22:20875670 | C | T | 3 | a0002c0003t0010g0248 a0002c0003t0010g0249 a0002c0003t0010g0250 |
3 | HG01070.hp1 HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.434+5137C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875670 | |||||||
chr22:20875737 | T | C | 3 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0072g0215 |
3 | HG03041.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.434+5204T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875737 | |||||||
chr22:20875835 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.435-5214G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875835 | |||||||
chr22:20875869 | A | T | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.435-5180A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875869 | |||||||
chr22:20875870 | T | G | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.435-5179T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875870 | |||||||
chr22:20875870 | T | TG | 95 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0047 others(92): Show |
97 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.435-5172dupG | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20875870 | ||||||
chr22:20875876 | G | C | 1 | a0001c0002t0002g0290 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.435-5173G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875876 | |||||||
chr22:20875889 | A | G | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.435-5160A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875889 | |||||||
chr22:20875898 | C | T | 1 | a0002c0003t0010g0254 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.435-5151C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875898 | |||||||
chr22:20875899 | G | T | 3 | a0001c0001t0003g0138 a0001c0001t0003g0143 a0001c0001t0003g0149 |
3 | HG01074.hp1 HG01123.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.435-5150G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875899 | |||||||
chr22:20875912 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.435-5137G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875912 | |||||||
chr22:20875969 | A | G | 34 | a0001c0002t0004g0204 a0001c0002t0004g0229 a0001c0002t0004g0230 others(31): Show |
34 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.435-5080A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875969 | |||||||
chr22:20875977 | C | T | 1 | a0001c0002t0005g0218 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.435-5072C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875977 | |||||||
chr22:20875983 | A | C | 1 | a0001c0001t0039g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.435-5066A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875983 | |||||||
chr22:20875983 | A | G | 1 | a0001c0001t0003g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.435-5066A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20875983 | |||||||
chr22:20876078 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.435-4971A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876078 | |||||||
chr22:20876156 | C | CA | 6 | a0001c0001t0001g0052 a0001c0001t0007g0033 a0001c0002t0005g0262 others(3): Show |
6 | HG01346.hp1 HG01346.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-4881dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876156 | ||||||
chr22:20876197 | G | A | 1 | a0001c0002t0002g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.435-4852G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876197 | |||||||
chr22:20876224 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.435-4825A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876224 | |||||||
chr22:20876255 | C | CT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0077 others(11): Show |
14 | HG00438.hp1 HG00609.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.435-4774dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876255 | ||||||
chr22:20876255 | C | G | 1 | a0001c0001t0029g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.435-4794C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876255 | |||||||
chr22:20876255 | CT | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
109 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.435-4774delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876255 | ||||||
chr22:20876255 | CTT | C | 46 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(43): Show |
48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.435-4775_435-4774d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876255 | ||||||
chr22:20876496 | G | C | 16 | a0002c0003t0010g0013 a0002c0003t0010g0248 a0002c0003t0010g0249 others(13): Show |
17 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.435-4553G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876496 | |||||||
chr22:20876568 | C | CT | 21 | a0001c0001t0001g0051 a0001c0001t0001g0086 a0001c0001t0001g0093 others(18): Show |
21 | HG00673.hp1 HG01978.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.435-4464dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876568 | ||||||
chr22:20876568 | C | CTT | 13 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(10): Show |
14 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.435-4465_435-4464d others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876568 | ||||||
chr22:20876568 | CT | C | 7 | a0001c0001t0009g0021 a0001c0001t0009g0180 a0001c0001t0009g0182 others(4): Show |
8 | HG02015.hp1 HG02055.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.435-4464delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20876568 | ||||||
chr22:20876613 | G | A | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.435-4436G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876613 | |||||||
chr22:20876636 | C | G | 1 | a0001c0001t0020g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.435-4413C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876636 | |||||||
chr22:20876637 | G | C | 1 | a0001c0001t0020g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.435-4412G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876637 | |||||||
chr22:20876649 | G | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
156 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.435-4400G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876649 | |||||||
chr22:20876716 | C | T | 1 | a0002c0003t0080g0321 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.435-4333C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20876716 | |||||||
chr22:20877131 | T | G | 2 | a0001c0002t0006g0288 a0001c0002t0068g0307 |
2 | NA18941.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.435-3918T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877131 | |||||||
chr22:20877197 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0046 others(9): Show |
13 | HG01261.hp1 HG01943.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.435-3852C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877197 | |||||||
chr22:20877429 | A | G | 1 | a0001c0001t0003g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.435-3620A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877429 | |||||||
chr22:20877573 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0076 a0001c0001t0001g0084 others(2): Show |
6 | HG01074.hp2 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.435-3476G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877573 | |||||||
chr22:20877584 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.435-3465C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877584 | |||||||
chr22:20877637 | A | G | 3 | a0001c0002t0012g0224 a0001c0002t0014g0245 a0001c0002t0075g0186 |
3 | NA18979.hp2 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.435-3412A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877637 | |||||||
chr22:20877711 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.435-3338G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877711 | |||||||
chr22:20877769 | A | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(17): Show |
22 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.435-3280A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20877769 | |||||||
chr22:20878022 | C | G | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.435-3027C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878022 | |||||||
chr22:20878431 | A | T | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.435-2618A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878431 | |||||||
chr22:20878434 | C | T | 1 | a0001c0001t0078g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.435-2615C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878434 | |||||||
chr22:20878468 | C | G | 13 | a0002c0003t0010g0013 a0002c0003t0010g0251 a0002c0003t0010g0254 others(10): Show |
14 | HG00423.hp2 HG00609.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.435-2581C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878468 | |||||||
chr22:20878648 | C | T | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.435-2401C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878648 | |||||||
chr22:20878838 | C | CAG | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.435-2211_435-2210i others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878838 | |||||||
chr22:20878969 | A | G | 5 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0039g0238 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.435-2080A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878969 | |||||||
chr22:20878982 | C | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(190): Show |
216 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.435-2067C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20878982 | |||||||
chr22:20879001 | A | G | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.435-2048A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879001 | |||||||
chr22:20879025 | T | C | 4 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0072g0215 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-2024T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879025 | |||||||
chr22:20879033 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.435-2016T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879033 | |||||||
chr22:20879034 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.435-2015G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879034 | |||||||
chr22:20879036 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.435-2013A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879036 | |||||||
chr22:20879083 | G | A | 2 | a0001c0001t0034g0202 a0001c0001t0034g0203 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.435-1966G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879083 | |||||||
chr22:20879112 | T | C | 1 | a0001c0001t0020g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.435-1937T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879112 | |||||||
chr22:20879114 | C | T | 1 | a0001c0001t0020g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.435-1935C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879114 | |||||||
chr22:20879123 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.435-1926C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879123 | |||||||
chr22:20879132 | C | G | 1 | a0001c0002t0005g0260 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.435-1917C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879132 | |||||||
chr22:20879140 | C | T | 2 | a0001c0001t0051g0034 a0001c0002t0014g0205 |
2 | HG02818.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.435-1909C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879140 | |||||||
chr22:20879159 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.435-1890T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879159 | |||||||
chr22:20879163 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.435-1886C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879163 | |||||||
chr22:20879168 | G | A | 1 | a0001c0002t0002g0284 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.435-1881G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879168 | |||||||
chr22:20879261 | C | T | 30 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(27): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.435-1788C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879261 | |||||||
chr22:20879294 | G | A | 1 | a0001c0002t0002g0285 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.435-1755G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879294 | |||||||
chr22:20879306 | C | CA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0169 a0001c0001t0020g0065 others(4): Show |
7 | HG01981.hp2 HG02027.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.435-1726dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20879306 | ||||||
chr22:20879306 | CA | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0083 a0001c0001t0001g0100 others(3): Show |
6 | HG00558.hp2 HG01346.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-1726delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20879306 | ||||||
chr22:20879439 | T | C | 6 | a0001c0001t0013g0011 a0001c0001t0013g0197 a0001c0001t0029g0198 others(3): Show |
7 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.435-1610T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879439 | |||||||
chr22:20879474 | G | A | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.435-1575G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879474 | |||||||
chr22:20879496 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0093 |
2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.435-1553G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879496 | |||||||
chr22:20879642 | T | G | 1 | a0001c0001t0003g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.435-1407T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879642 | |||||||
chr22:20879701 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.435-1348C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879701 | |||||||
chr22:20879826 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.435-1223G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879826 | |||||||
chr22:20879850 | TTAA | T | 29 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(26): Show |
30 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.435-1198_435-1196d others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879850 | |||||||
chr22:20879851 | T | A | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.435-1198T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879851 | |||||||
chr22:20879851 | T | TA | 13 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(10): Show |
14 | HG00741.hp2 HG02015.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.435-1174dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20879851 | ||||||
chr22:20879851 | TA | T | 7 | a0001c0001t0013g0011 a0001c0002t0006g0311 a0001c0002t0023g0313 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-1174delA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20879851 | ||||||
chr22:20879851 | TAAAA | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(128): Show |
150 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.435-1177_435-1174d others(6): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20879851 | ||||||
chr22:20879926 | G | A | 1 | a0001c0002t0015g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.435-1123G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20879926 | |||||||
chr22:20880013 | A | AAAC | 282 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(279): Show |
307 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.435-1024_435-1022d others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20880013 | ||||||
chr22:20880048 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435-1001A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880048 | |||||||
chr22:20880398 | C | T | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.435-651C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880398 | |||||||
chr22:20880505 | C | CA | 7 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0003g0159 others(4): Show |
7 | HG02451.hp1 HG02970.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-529dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 20880505 | ||||||
chr22:20880549 | G | A | 1 | a0001c0001t0058g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-500G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880549 | |||||||
chr22:20880549 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.435-500G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880549 | |||||||
chr22:20880580 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02129.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.435-469T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880580 | |||||||
chr22:20880652 | G | A | 7 | a0001c0002t0004g0214 a0001c0002t0004g0239 a0001c0002t0011g0209 others(4): Show |
7 | HG02622.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.435-397G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880652 | |||||||
chr22:20880766 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.435-283A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880766 | |||||||
chr22:20880808 | A | T | 1 | a0001c0002t0052g0211 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.435-241A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 2/4 | chr22 | 20880808 | |||||||
chr22:20881211 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.520+77G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881211 | |||||||
chr22:20881348 | C | G | 3 | a0001c0001t0029g0194 a0001c0001t0053g0022 a0001c0001t0054g0022 |
3 | HG02970.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.520+214C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881348 | |||||||
chr22:20881443 | C | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
156 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.520+309C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881443 | |||||||
chr22:20881550 | C | CA | 28 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.520+423dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 20881550 | ||||||
chr22:20881634 | G | A | 1 | a0001c0002t0014g0242 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.520+500G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881634 | |||||||
chr22:20881635 | A | G | 1 | a0001c0002t0014g0242 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.520+501A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881635 | |||||||
chr22:20881853 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(113): Show |
134 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.520+719C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881853 | |||||||
chr22:20881890 | C | A | 1 | a0001c0002t0011g0209 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520+756C>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20881890 | |||||||
chr22:20882084 | G | A | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.520+950G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882084 | |||||||
chr22:20882271 | G | A | 1 | a0001c0002t0004g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.520+1137G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882271 | |||||||
chr22:20882435 | T | G | 16 | a0001c0001t0013g0011 a0001c0001t0013g0191 a0001c0001t0013g0197 others(13): Show |
18 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.521-1036T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882435 | |||||||
chr22:20882588 | A | C | 1 | a0001c0001t0003g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.521-883A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882588 | |||||||
chr22:20882598 | A | G | 1 | a0001c0002t0011g0209 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.521-873A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882598 | |||||||
chr22:20882644 | G | T | 2 | a0001c0001t0034g0202 a0001c0001t0034g0203 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.521-827G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882644 | |||||||
chr22:20882892 | G | A | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.521-579G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882892 | |||||||
chr22:20882930 | T | C | 2 | a0001c0002t0002g0291 a0001c0002t0002g0295 |
2 | NA18967.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.521-541T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882930 | |||||||
chr22:20882984 | A | G | 3 | a0001c0001t0032g0023 a0001c0001t0066g0199 a0001c0001t0067g0200 |
4 | HG02145.hp2 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-487A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20882984 | |||||||
chr22:20882998 | C | CT | 53 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0009g0021 others(50): Show |
57 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.521-459dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 20882998 | ||||||
chr22:20882998 | CT | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0046 others(12): Show |
16 | HG01261.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.521-459delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 20882998 | ||||||
chr22:20883015 | G | A | 5 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0039g0238 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-456G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20883015 | |||||||
chr22:20883077 | T | C | 1 | a0001c0001t0030g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.521-394T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20883077 | |||||||
chr22:20883112 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.521-359T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20883112 | |||||||
chr22:20883130 | T | C | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.521-341T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20883130 | |||||||
chr22:20883356 | A | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0117 |
3 | HG00099.hp2 HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.521-115A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20883356 | |||||||
chr22:20883357 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0117 |
3 | HG00099.hp2 HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.521-114C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 3/4 | chr22 | 20883357 | |||||||
chr22:20883583 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.619+14C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20883583 | |||||||
chr22:20883933 | G | A | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.619+364G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20883933 | |||||||
chr22:20884015 | C | T | 1 | a0001c0002t0016g0293 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.619+446C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884015 | |||||||
chr22:20884059 | G | A | 1 | a0001c0002t0002g0286 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.619+490G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884059 | |||||||
chr22:20884186 | A | G | 1 | a0001c0001t0078g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.619+617A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884186 | |||||||
chr22:20884221 | T | A | 1 | a0001c0001t0049g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.619+652T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884221 | |||||||
chr22:20884304 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0001g0103 others(2): Show |
6 | HG00735.hp2 HG01934.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.619+735C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884304 | |||||||
chr22:20884331 | T | TA | 15 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0039g0238 others(12): Show |
15 | HG00738.hp1 HG01255.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.619+777dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20884331 | ||||||
chr22:20884377 | T | A | 1 | a0001c0002t0071g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.619+808T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884377 | |||||||
chr22:20884466 | G | A | 3 | a0001c0002t0004g0229 a0001c0002t0012g0231 a0001c0002t0012g0233 |
3 | HG03017.hp1 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.619+897G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884466 | |||||||
chr22:20884484 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.619+915G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884484 | |||||||
chr22:20884493 | G | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.619+924G>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884493 | |||||||
chr22:20884599 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02129.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.619+1030C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884599 | |||||||
chr22:20884633 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.619+1064C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884633 | |||||||
chr22:20884684 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.619+1115G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884684 | |||||||
chr22:20884765 | T | G | 1 | a0001c0001t0051g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.619+1196T>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884765 | |||||||
chr22:20884766 | A | ATGTTT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(132): Show |
154 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.619+1220_619+1224d others(7): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20884766 | ||||||
chr22:20884766 | A | ATGTTTTG others(3): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0103 |
3 | HG00735.hp2 HG01934.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.619+1215_619+1224d others(12): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20884766 | ||||||
chr22:20884825 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.619+1256C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884825 | |||||||
chr22:20884856 | A | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG02300.hp1 NA18971.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.619+1287A>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884856 | |||||||
chr22:20884858 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0102 a0001c0001t0001g0170 others(1): Show |
6 | NA18954.hp2 NA18955.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.619+1289C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884858 | |||||||
chr22:20884994 | C | T | 3 | a0001c0001t0026g0179 a0001c0001t0026g0181 a0001c0001t0044g0054 |
3 | HG02055.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.619+1425C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20884994 | |||||||
chr22:20885018 | G | A | 17 | a0001c0001t0049g0187 a0002c0003t0010g0013 a0002c0003t0010g0248 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.619+1449G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885018 | |||||||
chr22:20885040 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.619+1471G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885040 | |||||||
chr22:20885206 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.619+1637C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885206 | |||||||
chr22:20885227 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.619+1658C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885227 | |||||||
chr22:20885252 | C | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
218 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.619+1683C>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885252 | |||||||
chr22:20885252 | C | T | 2 | a0001c0002t0011g0232 a0001c0002t0011g0236 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.619+1683C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885252 | |||||||
chr22:20885276 | G | C | 1 | a0001c0002t0005g0259 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.619+1707G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885276 | |||||||
chr22:20885607 | G | C | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.619+2038G>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885607 | |||||||
chr22:20885740 | A | C | 1 | a0001c0001t0079g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-1939A>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885740 | |||||||
chr22:20885757 | G | A | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-1922G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885757 | |||||||
chr22:20885820 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
169 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.620-1859G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885820 | |||||||
chr22:20885827 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.620-1852T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20885827 | |||||||
chr22:20886110 | A | ACC | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(95): Show |
115 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.620-1569_620-1568i others(4): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886110 | |||||||
chr22:20886110 | A | ACCT | 35 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0035 others(32): Show |
38 | HG00423.hp2 HG00609.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.620-1569_620-1568i others(5): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886110 | |||||||
chr22:20886111 | T | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(50): Show |
55 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.620-1568T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886111 | |||||||
chr22:20886112 | C | CT | 32 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(29): Show |
34 | HG01167.hp1 HG01243.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.620-1553dupT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20886112 | ||||||
chr22:20886112 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(130): Show |
153 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.620-1567C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886112 | |||||||
chr22:20886112 | CT | C | 30 | a0001c0001t0013g0011 a0001c0001t0013g0191 a0001c0001t0013g0197 others(27): Show |
32 | HG01069.hp1 HG01891.hp1 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.620-1553delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20886112 | ||||||
chr22:20886126 | T | A | 30 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(27): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.620-1553T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886126 | |||||||
chr22:20886213 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
176 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.620-1466T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886213 | |||||||
chr22:20886318 | T | C | 1 | a0001c0002t0033g0278 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.620-1361T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886318 | |||||||
chr22:20886319 | A | G | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-1360A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886319 | |||||||
chr22:20886589 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.620-1090A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886589 | |||||||
chr22:20886635 | G | A | 1 | a0001c0002t0037g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.620-1044G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886635 | |||||||
chr22:20886851 | G | A | 1 | a0001c0001t0058g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.620-828G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886851 | |||||||
chr22:20886905 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
218 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.620-774A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886905 | |||||||
chr22:20886908 | C | T | 1 | a0001c0002t0002g0028 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.620-771C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886908 | |||||||
chr22:20886919 | A | G | 5 | a0001c0001t0030g0252 a0001c0001t0030g0253 a0001c0001t0039g0238 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.620-760A>G | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886919 | |||||||
chr22:20886945 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0007g0090 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.620-734C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886945 | |||||||
chr22:20886952 | G | A | 3 | a0001c0002t0002g0280 a0001c0002t0002g0287 a0001c0002t0002g0310 |
3 | HG00738.hp2 HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.620-727G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886952 | |||||||
chr22:20886961 | C | T | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-718C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20886961 | |||||||
chr22:20887082 | G | A | 3 | a0001c0001t0003g0156 a0001c0001t0025g0157 a0001c0001t0025g0158 |
3 | HG01433.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.620-597G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20887082 | |||||||
chr22:20887092 | G | A | 3 | a0001c0001t0078g0264 a0001c0002t0022g0222 a0001c0002t0022g0244 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.620-587G>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20887092 | |||||||
chr22:20887125 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.620-554T>A | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20887125 | |||||||
chr22:20887197 | C | T | 30 | a0001c0001t0003g0020 a0001c0001t0003g0053 a0001c0001t0003g0133 others(27): Show |
31 | HG00673.hp2 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.620-482C>T | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20887197 | |||||||
chr22:20887224 | C | CA | 56 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0088 others(53): Show |
58 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.620-441dupA | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20887224 | ||||||
chr22:20887468 | T | TAC | 9 | a0001c0001t0009g0021 a0001c0001t0009g0178 a0001c0001t0009g0180 others(6): Show |
10 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-195_620-194dup others(2): Show |
SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 20887468 | ||||||
chr22:20887565 | GT | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0046 others(8): Show |
12 | HG01261.hp1 HG02145.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.620-113delT | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20887565 | |||||||
chr22:20887566 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(124): Show |
146 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.620-113T>C | SNAP29 | ENSG00000099940.12 | transcript | ENST00000215730.12 | protein_coding | 4/4 | chr22 | 20887566 |