geneid | 80306 |
---|---|
ensemblid | ENSG00000118579.13 |
hgncid | 24628 |
symbol | MED28 |
name | mediator complex subunit 28 |
refseq_nuc | NM_025205.5 |
refseq_prot | NP_079481.2 |
ensembl_nuc | ENST00000237380.12 |
ensembl_prot | ENSP00000237380.6 |
mane_status | MANE Select |
chr | chr4 |
start | 17614641 |
end | 17634105 |
strand | + |
ver | v1.2 |
region | chr4:17614641-17634105 |
region5000 | chr4:17609641-17639105 |
regionname0 | MED28_chr4_17614641_17634105 |
regionname5000 | MED28_chr4_17609641_17639105 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 178 | 328 | 98 | 70 | 106 | 14 | 38 | 66 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 537 | 322 | 94 | 70 | 104 | 14 | 38 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
c0002 | 0/0 | 537 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
c0003 | 0/0 | 537 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
c0004 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 10289 | 43 | 1 | 15 | 22 | 1 | 4 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0002 | 0/1 | 10293 | 27 | 3 | 7 | 10 | 2 | 4 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0003 | 0/0 | 10291 | 13 | 1 | 4 | 6 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0004 | 0/0 | 10295 | 10 | 0 | 5 | 3 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0005 | 0/0 | 10289 | 8 | 0 | 0 | 8 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0006 | 0/0 | 10326 | 7 | 0 | 3 | 2 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0007 | 0/0 | 10294 | 7 | 0 | 1 | 6 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0008 | 0/0 | 10289 | 6 | 3 | 1 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0009 | 0/0 | 10321 | 5 | 5 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0010 | 0/0 | 10320 | 5 | 5 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0011 | 0/0 | 10293 | 5 | 0 | 0 | 4 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0012 | 0/0 | 10308 | 4 | 2 | 0 | 0 | 2 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0013 | 0/0 | 10320 | 4 | 1 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0014 | 0/0 | 10321 | 4 | 0 | 2 | 1 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0015 | 0/0 | 10285 | 4 | 0 | 3 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0016 | 0/0 | 10297 | 4 | 0 | 0 | 3 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0017 | 0/0 | 10322 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0018 | 0/0 | 10291 | 3 | 0 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0019 | 0/0 | 10287 | 3 | 0 | 2 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0020 | 0/0 | 10292 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0021 | 0/0 | 10285 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0022 | 0/0 | 10286 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0023 | 0/0 | 10321 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0024 | 0/0 | 10309 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0025 | 0/0 | 10322 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0026 | 0/0 | 10323 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0027 | 0/0 | 10323 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0028 | 0/0 | 10299 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0029 | 0/0 | 10320 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0030 | 0/0 | 10300 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0031 | 0/0 | 10290 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0032 | 0/0 | 10311 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0033 | 0/0 | 10312 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0034 | 0/0 | 10319 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0035 | 0/0 | 10321 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0036 | 0/0 | 10285 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0037 | 0/0 | 10291 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0038 | 0/0 | 10289 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0039 | 0/0 | 10290 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0040 | 0/0 | 10291 | 2 | 0 | 1 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0041 | 0/0 | 10293 | 2 | 0 | 1 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0042 | 0/0 | 10293 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0043 | 0/0 | 10291 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0044 | 0/0 | 10286 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0045 | 0/0 | 10285 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0046 | 0/0 | 10286 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0047 | 0/0 | 10285 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0048 | 0/0 | 10350 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0049 | 0/0 | 10304 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0050 | 0/0 | 10301 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0051 | 0/0 | 10295 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0052 | 0/0 | 10323 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0053 | 0/0 | 10326 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0054 | 0/0 | 10304 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0055 | 0/0 | 10316 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0056 | 0/0 | 10326 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0057 | 0/0 | 10327 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0058 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0059 | 0/0 | 10323 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0060 | 0/0 | 10327 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0061 | 0/0 | 10320 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0062 | 0/0 | 10322 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0063 | 0/0 | 10322 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0064 | 1/0 | 10322 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0065 | 0/0 | 10322 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0066 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0067 | 0/0 | 10304 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0068 | 0/0 | 10324 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0069 | 0/0 | 10335 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0070 | 0/0 | 10324 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0071 | 0/0 | 10324 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0072 | 0/0 | 10322 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0073 | 0/0 | 10320 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0074 | 0/0 | 10297 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0075 | 0/0 | 10303 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0076 | 0/0 | 10305 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0077 | 0/0 | 10313 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0078 | 0/0 | 10315 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0079 | 0/0 | 10324 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0080 | 0/0 | 10326 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0081 | 0/0 | 10311 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0082 | 0/0 | 10326 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0083 | 0/0 | 10325 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0084 | 0/0 | 10323 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0085 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0086 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0087 | 0/0 | 10284 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0088 | 0/0 | 10294 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0089 | 0/0 | 10294 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0090 | 0/0 | 10300 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0091 | 0/0 | 10284 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0092 | 0/0 | 10289 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0093 | 0/0 | 10295 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0094 | 0/0 | 10299 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0095 | 0/0 | 10294 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0096 | 0/0 | 10306 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0097 | 0/0 | 10297 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0098 | 0/0 | 10288 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0099 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0100 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0101 | 0/0 | 10288 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0102 | 0/0 | 10291 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0103 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0104 | 0/0 | 10322 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0105 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0106 | 0/0 | 10289 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0107 | 0/0 | 10295 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0108 | 0/0 | 10299 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0109 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0110 | 0/0 | 10294 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0111 | 0/0 | 10296 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0112 | 0/0 | 10297 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0113 | 0/0 | 10301 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0114 | 0/0 | 10319 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0115 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0116 | 0/0 | 10293 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0117 | 0/0 | 10288 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0118 | 0/0 | 10291 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0119 | 0/0 | 10277 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0120 | 0/0 | 10285 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0121 | 0/0 | 10286 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0122 | 0/0 | 10285 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0123 | 0/0 | 10287 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0124 | 0/0 | 10288 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0125 | 0/0 | 10289 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0126 | 0/0 | 10289 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0127 | 0/0 | 10289 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0128 | 0/0 | 10288 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0129 | 0/0 | 10289 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0130 | 0/0 | 10291 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0131 | 0/0 | 10291 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0132 | 0/0 | 10295 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0133 | 0/0 | 10295 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0134 | 0/0 | 10295 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0135 | 0/0 | 10295 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0136 | 0/0 | 10297 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0137 | 0/0 | 10299 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0138 | 0/0 | 10301 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0139 | 0/0 | 10298 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0140 | 0/0 | 10296 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0141 | 0/0 | 10289 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0142 | 0/0 | 10295 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0143 | 0/0 | 10291 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0144 | 0/0 | 10289 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0145 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0146 | 0/0 | 10283 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0147 | 0/0 | 10283 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0148 | 0/0 | 10285 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0149 | 0/0 | 10278 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0150 | 0/0 | 10300 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0151 | 0/0 | 10295 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0152 | 0/0 | 10296 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0153 | 0/0 | 10335 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0154 | 0/0 | 10324 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0155 | 0/0 | 10318 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0156 | 0/0 | 10322 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0157 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
t0158 | 0/0 | 10326 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 82 | 7 | 13 | 47 | 3 | 11 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0002 | 0/0 | 39 | 6 | 9 | 12 | 3 | 9 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0003 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0004 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0005 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0006 | 0/0 | 9 | 0 | 4 | 0 | 1 | 4 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0007 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0008 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0017 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0031 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 537 | 322 | 94 | 70 | 104 | 14 | 38 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0002 | 0/0 | 537 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0003 | 0/0 | 537 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0004 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10825 | 42 | 1 | 15 | 21 | 1 | 4 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0002 | 0/1 | 10829 | 27 | 3 | 7 | 10 | 2 | 4 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0003 | 0/0 | 10827 | 12 | 1 | 4 | 5 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0004 | 0/0 | 10831 | 10 | 0 | 5 | 3 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0005 | 0/0 | 10825 | 8 | 0 | 0 | 8 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0006 | 0/0 | 10862 | 7 | 0 | 3 | 2 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0007 | 0/0 | 10830 | 7 | 0 | 1 | 6 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0008 | 0/0 | 10825 | 6 | 3 | 1 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0009 | 0/0 | 10857 | 5 | 5 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0010 | 0/0 | 10856 | 5 | 5 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0011 | 0/0 | 10829 | 5 | 0 | 0 | 4 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0012 | 0/0 | 10844 | 4 | 2 | 0 | 0 | 2 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0013 | 0/0 | 10856 | 4 | 1 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0014 | 0/0 | 10857 | 4 | 0 | 2 | 1 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0015 | 0/0 | 10821 | 4 | 0 | 3 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0016 | 0/0 | 10833 | 4 | 0 | 0 | 3 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0017 | 0/0 | 10858 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0018 | 0/0 | 10827 | 3 | 0 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0019 | 0/0 | 10823 | 3 | 0 | 2 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0021 | 0/0 | 10821 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0022 | 0/0 | 10822 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0023 | 0/0 | 10857 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0024 | 0/0 | 10845 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0025 | 0/0 | 10858 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0026 | 0/0 | 10859 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0027 | 0/0 | 10859 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0028 | 0/0 | 10835 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0029 | 0/0 | 10856 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0030 | 0/0 | 10836 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0031 | 0/0 | 10826 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0032 | 0/0 | 10847 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0033 | 0/0 | 10848 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0034 | 0/0 | 10855 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0035 | 0/0 | 10857 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0036 | 0/0 | 10821 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0037 | 0/0 | 10827 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0038 | 0/0 | 10825 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0039 | 0/0 | 10826 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0040 | 0/0 | 10827 | 2 | 0 | 1 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0041 | 0/0 | 10829 | 2 | 0 | 1 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0042 | 0/0 | 10829 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0043 | 0/0 | 10827 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0044 | 0/0 | 10822 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0045 | 0/0 | 10821 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0046 | 0/0 | 10822 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0047 | 0/0 | 10821 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0048 | 0/0 | 10886 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0049 | 0/0 | 10840 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0050 | 0/0 | 10837 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0051 | 0/0 | 10831 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0052 | 0/0 | 10859 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0053 | 0/0 | 10862 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0054 | 0/0 | 10840 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0055 | 0/0 | 10852 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0056 | 0/0 | 10862 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0057 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0058 | 0/0 | 10859 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0059 | 0/0 | 10859 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0060 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0061 | 0/0 | 10856 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0062 | 0/0 | 10858 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0063 | 0/0 | 10858 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0064 | 1/0 | 10858 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0065 | 0/0 | 10858 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0066 | 0/0 | 10856 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0067 | 0/0 | 10840 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0068 | 0/0 | 10860 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0069 | 0/0 | 10871 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0070 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0071 | 0/0 | 10860 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0072 | 0/0 | 10858 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0073 | 0/0 | 10856 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0074 | 0/0 | 10833 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0075 | 0/0 | 10839 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0076 | 0/0 | 10841 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0077 | 0/0 | 10849 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0078 | 0/0 | 10851 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0079 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0080 | 0/0 | 10862 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0081 | 0/0 | 10847 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0082 | 0/0 | 10862 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0083 | 0/0 | 10861 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0084 | 0/0 | 10859 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0085 | 0/0 | 10856 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0086 | 0/0 | 10857 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0087 | 0/0 | 10820 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0088 | 0/0 | 10830 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0089 | 0/0 | 10830 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0090 | 0/0 | 10836 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0091 | 0/0 | 10820 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0092 | 0/0 | 10825 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0093 | 0/0 | 10831 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0094 | 0/0 | 10835 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0095 | 0/0 | 10830 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0096 | 0/0 | 10842 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0097 | 0/0 | 10833 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0098 | 0/0 | 10824 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0099 | 0/0 | 10826 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0100 | 0/0 | 10826 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0101 | 0/0 | 10824 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0102 | 0/0 | 10827 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0103 | 0/0 | 10856 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0104 | 0/0 | 10858 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0105 | 0/0 | 10857 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0106 | 0/0 | 10825 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0107 | 0/0 | 10831 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0108 | 0/0 | 10835 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0109 | 0/0 | 10826 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0110 | 0/0 | 10830 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0111 | 0/0 | 10832 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0112 | 0/0 | 10833 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0113 | 0/0 | 10837 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0114 | 0/0 | 10855 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0115 | 0/0 | 10857 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0116 | 0/0 | 10829 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0117 | 0/0 | 10824 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0118 | 0/0 | 10827 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0119 | 0/0 | 10813 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0120 | 0/0 | 10821 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0121 | 0/0 | 10822 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0122 | 0/0 | 10821 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0123 | 0/0 | 10823 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0124 | 0/0 | 10824 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0125 | 0/0 | 10825 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0126 | 0/0 | 10825 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0127 | 0/0 | 10825 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0128 | 0/0 | 10824 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0129 | 0/0 | 10825 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0130 | 0/0 | 10827 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0131 | 0/0 | 10827 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0132 | 0/0 | 10831 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0133 | 0/0 | 10831 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0134 | 0/0 | 10831 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0135 | 0/0 | 10831 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0136 | 0/0 | 10833 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0137 | 0/0 | 10835 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0138 | 0/0 | 10837 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0140 | 0/0 | 10832 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0141 | 0/0 | 10825 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0142 | 0/0 | 10831 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0143 | 0/0 | 10827 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0144 | 0/0 | 10825 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0145 | 0/0 | 10826 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0146 | 0/0 | 10819 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0147 | 0/0 | 10819 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0148 | 0/0 | 10821 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0149 | 0/0 | 10814 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0150 | 0/0 | 10836 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0151 | 0/0 | 10831 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0152 | 0/0 | 10832 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0153 | 0/0 | 10871 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0154 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0155 | 0/0 | 10854 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0156 | 0/0 | 10858 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0157 | 0/0 | 10856 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0001t0158 | 0/0 | 10862 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0002t0020 | 0/0 | 10828 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0002t0139 | 0/0 | 10834 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0003t0001 | 0/0 | 10825 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0003t0003 | 0/0 | 10827 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
a0001c0004t0020 | 0/0 | 10828 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | copy fasta | chr4 | 17609641 | 17639105 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 1 | 7 | 6 | 1 | 2 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0001 | 0/1 | 11 | 1 | 0 | 8 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0001 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0017 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0004g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0005g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0006g0002 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0007g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0008g0001 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0008g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0009g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0010g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0011g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0012g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0012g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0013g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0014g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0014g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0015g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0015g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0015g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0016g0001 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0016g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0017g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0018g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0018g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0019g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0019g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0021g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0021g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0022g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0023g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0024g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0025g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0025g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0026g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0026g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0027g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0027g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0028g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0029g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0030g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0030g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0031g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0031g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0032g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0033g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0034g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0035g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0035g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0036g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0037g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0037g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0038g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0039g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0040g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0040g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0041g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0041g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0042g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0042g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0043g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0044g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0045g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0046g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0047g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0048g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0049g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0050g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0051g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0052g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0053g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0054g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0055g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0056g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0057g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0058g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0059g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0060g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0061g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0062g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0063g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0064g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0065g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0066g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0067g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0068g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0069g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0070g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0071g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0072g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0073g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0074g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0075g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0076g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0077g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0078g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0079g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0080g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0081g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0082g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0083g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0084g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0085g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0086g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0087g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0088g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0089g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0090g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0091g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0092g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0093g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0094g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0095g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0096g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0097g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0098g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0099g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0100g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0101g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0102g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0103g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0104g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0105g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0106g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0107g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0108g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0109g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0110g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0111g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0112g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0113g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0114g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0115g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0116g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0117g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0118g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0119g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0120g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0121g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0122g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0123g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0124g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0125g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0126g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0127g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0128g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0129g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0130g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0131g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0132g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0133g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0134g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0135g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0136g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0137g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0138g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0140g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0141g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0142g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0143g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0144g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0145g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0146g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0147g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0148g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0149g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0150g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0151g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0152g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0153g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0154g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0155g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0156g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0157g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0001t0158g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0002t0020g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0002t0139g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0003t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
a0001c0004t0020g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0033 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0001 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00140 | hp2 | a0001 | c0001 | t0014 | g0002 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0048 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0002 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00323 | hp1 | a0001 | c0001 | t0078 | g0002 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00423 | hp1 | a0001 | c0001 | t0055 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00438 | hp2 | a0001 | c0001 | t0138 | g0011 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00544 | hp1 | a0001 | c0001 | t0134 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00544 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00597 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00597 | hp2 | a0001 | c0001 | t0071 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00609 | hp2 | a0001 | c0001 | t0065 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00621 | hp1 | a0001 | c0001 | t0038 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00642 | hp1 | a0001 | c0001 | t0123 | g0006 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00673 | hp1 | a0001 | c0001 | t0059 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00733 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00735 | hp2 | a0001 | c0001 | t0027 | g0034 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00738 | hp1 | a0001 | c0001 | t0073 | g0034 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01069 | hp1 | a0001 | c0001 | t0015 | g0006 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01069 | hp2 | a0001 | c0001 | t0019 | g0014 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01071 | hp2 | a0001 | c0001 | t0019 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0002 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01081 | hp1 | a0001 | c0001 | t0052 | g0002 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01081 | hp2 | a0001 | c0001 | t0014 | g0035 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01109 | hp1 | a0001 | c0001 | t0033 | g0015 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01169 | hp2 | a0001 | c0001 | t0068 | g0090 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01175 | hp1 | a0001 | c0001 | t0013 | g0093 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01192 | hp1 | a0001 | c0001 | t0018 | g0005 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01192 | hp2 | a0001 | c0001 | t0119 | g0011 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01243 | hp1 | a0001 | c0001 | t0147 | g0023 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01243 | hp2 | a0001 | c0001 | t0087 | g0103 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01255 | hp2 | a0001 | c0001 | t0054 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01257 | hp1 | a0001 | c0001 | t0027 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01261 | hp1 | a0001 | c0001 | t0041 | g0046 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01261 | hp2 | a0001 | c0001 | t0118 | g0001 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0094 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01358 | hp1 | a0001 | c0001 | t0014 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01358 | hp2 | a0001 | c0001 | t0053 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01361 | hp2 | a0001 | c0001 | t0026 | g0092 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01433 | hp2 | a0001 | c0001 | t0015 | g0019 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01496 | hp1 | a0001 | c0001 | t0122 | g0008 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01516 | hp1 | a0001 | c0001 | t0012 | g0033 | EUR | IBS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01516 | hp2 | a0001 | c0001 | t0121 | g0006 | EUR | IBS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01884 | hp1 | a0001 | c0001 | t0084 | g0091 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01884 | hp2 | a0001 | c0001 | t0033 | g0015 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01952 | hp1 | a0001 | c0001 | t0018 | g0005 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01975 | hp2 | a0001 | c0001 | t0126 | g0037 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02015 | hp1 | a0001 | c0001 | t0015 | g0049 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02015 | hp2 | a0001 | c0001 | t0109 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02027 | hp1 | a0001 | c0001 | t0038 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02027 | hp2 | a0001 | c0001 | t0082 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02055 | hp1 | a0001 | c0001 | t0035 | g0078 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02055 | hp2 | a0001 | c0001 | t0067 | g0089 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02074 | hp1 | a0001 | c0001 | t0107 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02129 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02132 | hp1 | a0001 | c0001 | t0081 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02132 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02135 | hp1 | a0001 | c0001 | t0083 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02135 | hp2 | a0001 | c0001 | t0131 | g0019 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02145 | hp1 | a0001 | c0001 | t0029 | g0003 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02145 | hp2 | a0001 | c0001 | t0051 | g0065 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02148 | hp1 | a0001 | c0001 | t0127 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02155 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | CDX | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02257 | hp1 | a0001 | c0001 | t0150 | g0064 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02258 | hp2 | a0001 | c0001 | t0103 | g0032 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02280 | hp1 | a0001 | c0001 | t0113 | g0012 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02280 | hp2 | a0001 | c0001 | t0032 | g0015 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02293 | hp2 | a0001 | c0001 | t0026 | g0002 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02300 | hp1 | a0001 | c0001 | t0116 | g0040 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02451 | hp1 | a0001 | c0001 | t0021 | g0070 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02451 | hp2 | a0001 | c0001 | t0157 | g0028 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02523 | hp2 | a0001 | c0001 | t0039 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02572 | hp1 | a0001 | c0001 | t0024 | g0002 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02572 | hp2 | a0001 | c0001 | t0149 | g0073 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02602 | hp1 | a0001 | c0001 | t0011 | g0052 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02615 | hp1 | a0001 | c0001 | t0146 | g0038 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02615 | hp2 | a0001 | c0001 | t0088 | g0105 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02622 | hp2 | a0001 | c0001 | t0058 | g0030 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02630 | hp1 | a0001 | c0001 | t0045 | g0020 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02630 | hp2 | a0001 | c0001 | t0032 | g0015 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02647 | hp2 | a0001 | c0001 | t0060 | g0030 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02698 | hp1 | a0001 | c0001 | t0061 | g0088 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02698 | hp2 | a0001 | c0001 | t0135 | g0025 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02717 | hp1 | a0001 | c0001 | t0034 | g0009 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02717 | hp2 | a0001 | c0001 | t0132 | g0044 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02723 | hp1 | a0001 | c0001 | t0023 | g0002 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02735 | hp2 | a0001 | c0001 | t0128 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02738 | hp1 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02809 | hp2 | a0001 | c0001 | t0029 | g0003 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02818 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02818 | hp2 | a0001 | c0001 | t0028 | g0003 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02886 | hp1 | a0001 | c0001 | t0049 | g0082 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02895 | hp2 | a0001 | c0001 | t0148 | g0023 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02896 | hp2 | a0001 | c0001 | t0115 | g0012 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02897 | hp2 | a0001 | c0001 | t0114 | g0012 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02922 | hp1 | a0001 | c0001 | t0090 | g0104 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02922 | hp2 | a0001 | c0001 | t0035 | g0009 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02965 | hp1 | a0001 | c0001 | t0050 | g0022 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02970 | hp1 | a0001 | c0002 | t0139 | g0013 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02970 | hp2 | a0001 | c0001 | t0048 | g0097 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02976 | hp1 | a0001 | c0001 | t0066 | g0002 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02976 | hp2 | a0001 | c0002 | t0020 | g0013 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03017 | hp2 | a0001 | c0001 | t0152 | g0072 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03041 | hp1 | a0001 | c0002 | t0020 | g0013 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03041 | hp2 | a0001 | c0001 | t0111 | g0012 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03098 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03098 | hp2 | a0001 | c0001 | t0155 | g0027 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03130 | hp1 | a0001 | c0001 | t0062 | g0002 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03130 | hp2 | a0001 | c0004 | t0020 | g0013 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03139 | hp1 | a0001 | c0001 | t0028 | g0084 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03139 | hp2 | a0001 | c0001 | t0085 | g0003 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03195 | hp1 | a0001 | c0001 | t0034 | g0009 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03195 | hp2 | a0001 | c0001 | t0037 | g0061 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03209 | hp2 | a0001 | c0001 | t0158 | g0028 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03225 | hp1 | a0001 | c0001 | t0086 | g0003 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03225 | hp2 | a0001 | c0001 | t0047 | g0020 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03239 | hp1 | a0001 | c0001 | t0040 | g0025 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03453 | hp1 | a0001 | c0001 | t0037 | g0001 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0075 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03486 | hp1 | a0001 | c0001 | t0091 | g0036 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03486 | hp2 | a0001 | c0001 | t0044 | g0067 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03490 | hp1 | a0001 | c0001 | t0074 | g0086 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03490 | hp2 | a0001 | c0001 | t0036 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03491 | hp1 | a0001 | c0001 | t0042 | g0047 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03491 | hp2 | a0001 | c0001 | t0076 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03492 | hp1 | a0001 | c0001 | t0036 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03492 | hp2 | a0001 | c0001 | t0042 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03540 | hp1 | a0001 | c0001 | t0156 | g0027 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03579 | hp1 | a0001 | c0001 | t0046 | g0068 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03579 | hp2 | a0001 | c0001 | t0092 | g0016 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03654 | hp1 | a0001 | c0001 | t0153 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03654 | hp2 | a0001 | c0001 | t0143 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03704 | hp2 | a0001 | c0001 | t0025 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03710 | hp2 | a0001 | c0001 | t0154 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03831 | hp1 | a0001 | c0001 | t0133 | g0001 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03831 | hp2 | a0001 | c0001 | t0031 | g0080 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03927 | hp2 | a0001 | c0001 | t0120 | g0006 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03942 | hp1 | a0001 | c0001 | t0063 | g0002 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG04184 | hp1 | a0001 | c0001 | t0025 | g0095 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG04184 | hp2 | a0001 | c0001 | t0070 | g0002 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG04199 | hp1 | a0001 | c0001 | t0031 | g0005 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG04199 | hp2 | a0001 | c0001 | t0072 | g0002 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG04228 | hp2 | a0001 | c0001 | t0075 | g0002 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18522 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18522 | hp2 | a0001 | c0001 | t0021 | g0066 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18612 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | CHB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | CHB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18906 | hp1 | a0001 | c0001 | t0096 | g0016 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18906 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18939 | hp1 | a0001 | c0001 | t0151 | g0071 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18945 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18946 | hp1 | a0001 | c0001 | t0141 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18946 | hp2 | a0001 | c0001 | t0077 | g0002 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18947 | hp1 | a0001 | c0001 | t0144 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18950 | hp1 | a0001 | c0001 | t0056 | g0002 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18950 | hp2 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18963 | hp1 | a0001 | c0001 | t0043 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18978 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18979 | hp1 | a0001 | c0001 | t0142 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18982 | hp1 | a0001 | c0001 | t0129 | g0050 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18991 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18991 | hp2 | a0001 | c0001 | t0136 | g0045 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18993 | hp1 | a0001 | c0001 | t0039 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18993 | hp2 | a0001 | c0001 | t0145 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18998 | hp2 | a0001 | c0001 | t0102 | g0021 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19000 | hp2 | a0001 | c0001 | t0099 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19004 | hp2 | a0001 | c0001 | t0106 | g0010 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19010 | hp2 | a0001 | c0001 | t0130 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19012 | hp2 | a0001 | c0001 | t0098 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19030 | hp1 | a0001 | c0001 | t0105 | g0079 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19030 | hp2 | a0001 | c0001 | t0022 | g0069 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19043 | hp1 | a0001 | c0001 | t0095 | g0099 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19043 | hp2 | a0001 | c0001 | t0093 | g0102 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19056 | hp1 | a0001 | c0001 | t0100 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19056 | hp2 | a0001 | c0001 | t0124 | g0010 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19057 | hp1 | a0001 | c0001 | t0110 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19058 | hp1 | a0001 | c0001 | t0101 | g0029 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19068 | hp1 | a0001 | c0001 | t0125 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19079 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19081 | hp1 | a0001 | c0001 | t0140 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19081 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19085 | hp1 | a0001 | c0001 | t0117 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19087 | hp2 | a0001 | c0001 | t0057 | g0002 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19088 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA19240 | hp2 | a0001 | c0001 | t0024 | g0002 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20129 | hp1 | a0001 | c0001 | t0112 | g0012 | AFR | ASW | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20129 | hp2 | a0001 | c0001 | t0069 | g0085 | AFR | ASW | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20752 | hp2 | a0001 | c0001 | t0079 | g0096 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20805 | hp2 | a0001 | c0001 | t0041 | g0008 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01123 | hp1 | a0001 | c0001 | t0040 | g0058 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG01123 | hp2 | a0001 | c0001 | t0018 | g0077 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02109 | hp1 | a0001 | c0001 | t0030 | g0016 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02486 | hp1 | a0001 | c0001 | t0010 | g0076 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02486 | hp2 | a0001 | c0001 | t0137 | g0001 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02559 | hp1 | a0001 | c0001 | t0104 | g0032 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG02559 | hp2 | a0001 | c0001 | t0094 | g0101 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03471 | hp1 | a0001 | c0001 | t0080 | g0031 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG03471 | hp2 | a0001 | c0001 | t0022 | g0020 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
HG06807 | hp2 | a0001 | c0001 | t0030 | g0100 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA18955 | hp2 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA20300 | hp2 | a0001 | c0001 | t0089 | g0036 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA21309 | hp1 | a0001 | c0001 | t0097 | g0016 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
NA21309 | hp2 | a0001 | c0001 | t0108 | g0055 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0064 | g0031 | REF | REF | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:17614663
|
T | C | 1 | a0001c0003 | 2 | NA18959.hp2 NA19088.hp2 |
synonymous_variant | LOW | c.9T>C | p.Ala3Ala | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/4 | 23/10858 | 9/537 | 3/178 | chr4 | 17614663 | ||
chr4:17614726
|
G | A | 2 | a0001c0002a0001c0004 | 4 | HG02970.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.72G>A | p.Pro24Pro | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/4 | 86/10858 | 72/537 | 24/178 | chr4 | 17614726 | ||
chr4:17619930
|
C | T | 1 | a0001c0004 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.189C>T | p.Asp63Asp | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/4 | 203/10858 | 189/537 | 63/178 | chr4 | 17619930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:17623888
|
C | A | 1 | a0001c0001t0043 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 90 | chr4 | 17623888 | |||||
chr4:17624015
|
A | AT | 13 | a0001c0001t0146a0001c0001t0147a0001c0001t0148others(10): Show | 13 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*227dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 228 | INFO_REALIGN_3_PRIME | chr4 | 17624015 | ||||
chr4:17624035
|
A | G | 66 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(63): Show | 184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*237A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 237 | chr4 | 17624035 | |||||
chr4:17624125
|
G | A | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*327G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 327 | chr4 | 17624125 | |||||
chr4:17624168
|
C | T | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0018others(13): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*370C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 370 | chr4 | 17624168 | |||||
chr4:17624184
|
T | C | 4 | a0001c0001t0012a0001c0001t0048a0001c0001t0049others(1): Show | 7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*386T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 386 | chr4 | 17624184 | |||||
chr4:17624236
|
A | G | 8 | a0001c0001t0010a0001c0001t0032a0001c0001t0033others(5): Show | 16 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*438A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 438 | chr4 | 17624236 | |||||
chr4:17624272
|
C | T | 12 | a0001c0001t0030a0001c0001t0087a0001c0001t0088others(9): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*474C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 474 | chr4 | 17624272 | |||||
chr4:17624360
|
G | A | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*562G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 562 | chr4 | 17624360 | |||||
chr4:17624374
|
G | A | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 576 | chr4 | 17624374 | |||||
chr4:17624471
|
G | C | 1 | a0001c0001t0087 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*673G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 673 | chr4 | 17624471 | |||||
chr4:17624551
|
T | A | 96 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(93): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*753T>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 753 | chr4 | 17624551 | |||||
chr4:17624554
|
CTG | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*758_*759delGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 758 | INFO_REALIGN_3_PRIME | chr4 | 17624554 | ||||
chr4:17624633
|
T | G | 1 | a0001c0001t0149 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*835T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 835 | chr4 | 17624633 | |||||
chr4:17624646
|
C | T | 7 | a0001c0001t0030a0001c0001t0092a0001c0001t0093others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*848C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 848 | chr4 | 17624646 | |||||
chr4:17624674
|
G | T | 1 | a0001c0001t0152 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*876G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 876 | chr4 | 17624674 | |||||
chr4:17624740
|
C | T | 1 | a0001c0001t0047 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 942 | chr4 | 17624740 | |||||
chr4:17624760
|
G | A | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0031others(5): Show | 18 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*962G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 962 | chr4 | 17624760 | |||||
chr4:17624795
|
G | A | 112 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(109): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 997 | chr4 | 17624795 | |||||
chr4:17624861
|
A | T | 2 | a0001c0001t0144a0001c0001t0145 | 2 | NA18947.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1063A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1063 | chr4 | 17624861 | |||||
chr4:17624930
|
A | G | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1132A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1132 | chr4 | 17624930 | |||||
chr4:17625097
|
C | T | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1299C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1299 | chr4 | 17625097 | |||||
chr4:17625172
|
G | C | 1 | a0001c0001t0106 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1374 | chr4 | 17625172 | |||||
chr4:17625223
|
G | A | 2 | a0001c0001t0052a0001c0001t0053 | 2 | HG01081.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1425G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1425 | chr4 | 17625223 | |||||
chr4:17625575
|
C | T | 1 | a0001c0001t0143 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1777C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1777 | chr4 | 17625575 | |||||
chr4:17625576
|
G | A | 4 | a0001c0001t0155a0001c0001t0156a0001c0001t0157others(1): Show | 4 | HG02451.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1778G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1778 | chr4 | 17625576 | |||||
chr4:17625671
|
A | G | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1873A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1873 | chr4 | 17625671 | |||||
chr4:17625709
|
T | C | 92 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*1911T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1911 | chr4 | 17625709 | |||||
chr4:17625850
|
G | A | 1 | a0001c0001t0116 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2052 | chr4 | 17625850 | |||||
chr4:17625962
|
C | A | 1 | a0001c0001t0054 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2164 | chr4 | 17625962 | |||||
chr4:17626053
|
C | T | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0018others(13): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2255C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2255 | chr4 | 17626053 | |||||
chr4:17626092
|
C | G | 2 | a0001c0001t0141a0001c0001t0142 | 2 | NA18946.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2294C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2294 | chr4 | 17626092 | |||||
chr4:17626131
|
G | T | 6 | a0001c0001t0097a0001c0001t0111a0001c0001t0112others(3): Show | 6 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2333G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2333 | chr4 | 17626131 | |||||
chr4:17626147
|
G | T | 6 | a0001c0001t0009a0001c0001t0017a0001c0001t0028others(3): Show | 14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2349G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2349 | chr4 | 17626147 | |||||
chr4:17626233
|
G | A | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*2435G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2435 | chr4 | 17626233 | |||||
chr4:17626328
|
G | A | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2530 | chr4 | 17626328 | |||||
chr4:17626413
|
T | C | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2615T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2615 | chr4 | 17626413 | |||||
chr4:17626460
|
G | C | 3 | a0001c0001t0055a0001c0001t0056a0001c0001t0057 | 3 | HG00423.hp1 NA18950.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2662G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2662 | chr4 | 17626460 | |||||
chr4:17626524
|
T | C | 1 | a0001c0001t0150 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2726 | chr4 | 17626524 | |||||
chr4:17626663
|
C | A | 4 | a0001c0001t0155a0001c0001t0156a0001c0001t0157others(1): Show | 4 | HG02451.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2865C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2865 | chr4 | 17626663 | |||||
chr4:17626678
|
C | CT | 11 | a0001c0001t0030a0001c0001t0051a0001c0001t0087others(8): Show | 12 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2890dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2891 | INFO_REALIGN_3_PRIME | chr4 | 17626678 | ||||
chr4:17626758
|
T | C | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2960T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2960 | chr4 | 17626758 | |||||
chr4:17626805
|
C | T | 7 | a0001c0001t0030a0001c0001t0092a0001c0001t0093others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3007C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3007 | chr4 | 17626805 | |||||
chr4:17626951
|
A | G | 6 | a0001c0001t0009a0001c0001t0017a0001c0001t0028others(3): Show | 14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3153A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3153 | chr4 | 17626951 | |||||
chr4:17626963
|
A | AT | 21 | a0001c0001t0005a0001c0001t0009a0001c0001t0010others(18): Show | 47 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3184dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3185 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | ||||
chr4:17626963
|
AT | A | 16 | a0001c0001t0007a0001c0001t0058a0001c0001t0059others(13): Show | 23 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3184delT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3184 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | ||||
chr4:17626963
|
ATT | A | 70 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(67): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*3183_*3184delTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3183 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | ||||
chr4:17626963
|
ATTT | A | 7 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(4): Show | 9 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3182_*3184delTTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3182 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | ||||
chr4:17627007
|
C | G | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*3209C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3209 | chr4 | 17627007 | |||||
chr4:17627064
|
A | G | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3266 | chr4 | 17627064 | |||||
chr4:17627073
|
C | G | 1 | a0001c0001t0087 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3275C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3275 | chr4 | 17627073 | |||||
chr4:17627107
|
C | T | 4 | a0001c0001t0149a0001c0001t0150a0001c0001t0151others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3309C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3309 | chr4 | 17627107 | |||||
chr4:17627115
|
C | T | 1 | a0001c0001t0110 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3317C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3317 | chr4 | 17627115 | |||||
chr4:17627146
|
T | C | 118 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(115): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*3348T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3348 | chr4 | 17627146 | |||||
chr4:17627164
|
G | C | 7 | a0001c0001t0146a0001c0001t0147a0001c0001t0148others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3366G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3366 | chr4 | 17627164 | |||||
chr4:17627167
|
A | G | 4 | a0001c0001t0149a0001c0001t0150a0001c0001t0151others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3369A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3369 | chr4 | 17627167 | |||||
chr4:17627196
|
G | A | 4 | a0001c0001t0012a0001c0001t0048a0001c0001t0049others(1): Show | 7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3398G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3398 | chr4 | 17627196 | |||||
chr4:17627243
|
G | A | 5 | a0001c0001t0038a0001c0001t0149a0001c0001t0150others(2): Show | 6 | HG00621.hp1 HG02027.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3445G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3445 | chr4 | 17627243 | |||||
chr4:17627334
|
T | C | 2 | a0001c0001t0116a0001c0001t0118 | 2 | HG01261.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3536T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3536 | chr4 | 17627334 | |||||
chr4:17627364
|
A | G | 1 | a0001c0001t0042 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3566A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3566 | chr4 | 17627364 | |||||
chr4:17627475
|
CTG | C | 16 | a0001c0001t0005a0001c0001t0010a0001c0001t0018others(13): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3679_*3680delGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3679 | INFO_REALIGN_3_PRIME | chr4 | 17627475 | ||||
chr4:17627536
|
G | A | 2 | a0001c0001t0155a0001c0001t0156 | 2 | HG03098.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3738 | chr4 | 17627536 | |||||
chr4:17627626
|
C | G | 1 | a0001c0001t0051 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3828C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3828 | chr4 | 17627626 | |||||
chr4:17627719
|
C | A | 4 | a0001c0001t0012a0001c0001t0048a0001c0001t0049others(1): Show | 7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3921C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3921 | chr4 | 17627719 | |||||
chr4:17627722
|
A | G | 7 | a0001c0001t0012a0001c0001t0048a0001c0001t0049others(4): Show | 10 | HG00099.hp2 HG01243.hp1 HG01516.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3924A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3924 | chr4 | 17627722 | |||||
chr4:17627739
|
G | C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3941G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3941 | chr4 | 17627739 | |||||
chr4:17627926
|
G | C | 5 | a0001c0001t0087a0001c0001t0088a0001c0001t0089others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4128G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4128 | chr4 | 17627926 | |||||
chr4:17627941
|
A | G | 1 | a0001c0001t0152 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4143A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4143 | chr4 | 17627941 | |||||
chr4:17627943
|
C | T | 1 | a0001c0001t0105 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4145C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4145 | chr4 | 17627943 | |||||
chr4:17628121
|
A | G | 2 | a0001c0001t0151a0001c0001t0152 | 2 | HG03017.hp2 NA18939.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4323A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4323 | chr4 | 17628121 | |||||
chr4:17628175
|
G | A | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0031others(5): Show | 18 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4377G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4377 | chr4 | 17628175 | |||||
chr4:17628249
|
A | G | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4451A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4451 | chr4 | 17628249 | |||||
chr4:17628255
|
C | CGT | 24 | a0001c0001t0013a0001c0001t0014a0001c0001t0019others(21): Show | 35 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4492_*4493dupGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGT | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(36): Show | 101 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*4490_*4493dupGTGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGT | 17 | a0001c0001t0003a0001c0001t0037a0001c0001t0040others(14): Show | 31 | HG00323.hp2 HG00621.hp2 HG01123.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4488_*4493dupGTGT others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(1): Show |
10 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(7): Show | 48 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4486_*4493dupGTGT others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(3): Show |
12 | a0001c0001t0004a0001c0001t0030a0001c0001t0094others(9): Show | 22 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4484_*4493dupGTGT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(5): Show |
3 | a0001c0001t0016a0001c0001t0136a0001c0002t0139 | 6 | HG00140.hp1 HG02970.hp1 NA18945.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4482_*4493dupGTGT others(8): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(7): Show |
3 | a0001c0001t0108a0001c0001t0113a0001c0001t0137 | 3 | HG02280.hp1 HG02486.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4480_*4493dupGTGT others(10): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(9): Show |
2 | a0001c0001t0096a0001c0001t0138 | 2 | HG00438.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4478_*4493dupGTGT others(12): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(23): Show |
1 | a0001c0001t0155 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4464_*4493dupGTGT others(26): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(25): Show |
2 | a0001c0001t0114a0001c0001t0157 | 2 | HG02451.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4462_*4493dupGTGT others(28): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(27): Show |
2 | a0001c0001t0115a0001c0001t0156 | 2 | HG02896.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4460_*4493dupGTGT others(30): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
C | CGTGTGTG others(31): Show |
1 | a0001c0001t0158 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4493_*4494insGTGT others(34): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
CGTGTGTG others(1): Show |
C | 11 | a0001c0001t0018a0001c0001t0021a0001c0001t0022others(8): Show | 15 | HG01123.hp2 HG01192.hp1 HG01192.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4486_*4493delGTGT others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4486 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
CGTGTGTG others(3): Show |
C | 10 | a0001c0001t0005a0001c0001t0031a0001c0001t0032others(7): Show | 20 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4484_*4493delGTGT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4484 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628255
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0149 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4476_*4493delGTGT others(14): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4476 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | ||||
chr4:17628280
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4493_*4494insGTGT others(18): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628280 | ||||
chr4:17628282
|
G | A | 3 | a0001c0001t0012a0001c0001t0049a0001c0001t0050 | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4484G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4484 | chr4 | 17628282 | |||||
chr4:17628290
|
G | A | 1 | a0001c0001t0018 | 3 | HG01123.hp2 HG01192.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4492G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4492 | chr4 | 17628290 | |||||
chr4:17628292
|
A | G | 3 | a0001c0001t0012a0001c0001t0049a0001c0001t0050 | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4494A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | chr4 | 17628292 | |||||
chr4:17628307
|
T | C | 1 | a0001c0001t0125 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4509T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4509 | chr4 | 17628307 | |||||
chr4:17628316
|
A | G | 78 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(75): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*4518A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4518 | chr4 | 17628316 | |||||
chr4:17628326
|
GTA | G | 7 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(4): Show | 9 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4538_*4539delAT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4538 | INFO_REALIGN_3_PRIME | chr4 | 17628326 | ||||
chr4:17628328
|
A | G | 1 | a0001c0001t0073 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4530A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4530 | chr4 | 17628328 | |||||
chr4:17628332
|
A | G | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4534A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4534 | chr4 | 17628332 | |||||
chr4:17628334
|
A | G | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4536A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4536 | chr4 | 17628334 | |||||
chr4:17628336
|
A | G | 3 | a0001c0001t0012a0001c0001t0048a0001c0001t0050 | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4538A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4538 | chr4 | 17628336 | |||||
chr4:17628342
|
G | A | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4544G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4544 | chr4 | 17628342 | |||||
chr4:17628344
|
G | A | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4546G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4546 | chr4 | 17628344 | |||||
chr4:17628344
|
G | GTATA | 2 | a0001c0001t0012a0001c0001t0050 | 5 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4547_*4548insATAT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4548 | INFO_REALIGN_3_PRIME | chr4 | 17628344 | ||||
chr4:17628346
|
G | A | 3 | a0001c0001t0012a0001c0001t0048a0001c0001t0050 | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4548G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4548 | chr4 | 17628346 | |||||
chr4:17628451
|
G | A | 1 | a0001c0001t0082 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4653G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4653 | chr4 | 17628451 | |||||
chr4:17628461
|
T | C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4663T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4663 | chr4 | 17628461 | |||||
chr4:17628462
|
CACTTCCT others(3): Show |
C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4666_*4675delCTTC others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4666 | INFO_REALIGN_3_PRIME | chr4 | 17628462 | ||||
chr4:17628474
|
A | G | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4676A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4676 | chr4 | 17628474 | |||||
chr4:17628487
|
G | T | 1 | a0001c0001t0150 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4689G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4689 | chr4 | 17628487 | |||||
chr4:17628492
|
G | A | 112 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(109): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*4694G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4694 | chr4 | 17628492 | |||||
chr4:17628539
|
A | G | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4741A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4741 | chr4 | 17628539 | |||||
chr4:17628569
|
G | T | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*4771G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4771 | chr4 | 17628569 | |||||
chr4:17628616
|
C | T | 1 | a0001c0001t0072 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4818C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4818 | chr4 | 17628616 | |||||
chr4:17628619
|
C | A | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*4821C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4821 | chr4 | 17628619 | |||||
chr4:17628652
|
C | T | 2 | a0001c0001t0022a0001c0001t0045 | 3 | HG02630.hp1 HG03471.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4854C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4854 | chr4 | 17628652 | |||||
chr4:17628686
|
A | G | 4 | a0001c0001t0149a0001c0001t0150a0001c0001t0151others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4888A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4888 | chr4 | 17628686 | |||||
chr4:17628920
|
C | A | 7 | a0001c0001t0146a0001c0001t0147a0001c0001t0148others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5122C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5122 | chr4 | 17628920 | |||||
chr4:17629063
|
C | T | 1 | a0001c0001t0151 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5265C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5265 | chr4 | 17629063 | |||||
chr4:17629071
|
C | G | 3 | a0001c0001t0012a0001c0001t0049a0001c0001t0050 | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5273C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5273 | chr4 | 17629071 | |||||
chr4:17629094
|
A | T | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*5296A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5296 | chr4 | 17629094 | |||||
chr4:17629166
|
G | A | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG02698.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5368G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5368 | chr4 | 17629166 | |||||
chr4:17629210
|
G | T | 7 | a0001c0001t0030a0001c0001t0092a0001c0001t0093others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5412G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5412 | chr4 | 17629210 | |||||
chr4:17629234
|
AAAAC | A | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5442_*5445delAACA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5442 | INFO_REALIGN_3_PRIME | chr4 | 17629234 | ||||
chr4:17629263
|
G | T | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5465G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5465 | chr4 | 17629263 | |||||
chr4:17629318
|
C | G | 2 | a0001c0001t0040a0001c0001t0135 | 3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5520C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5520 | chr4 | 17629318 | |||||
chr4:17629326
|
T | C | 2 | a0001c0001t0052a0001c0001t0053 | 2 | HG01081.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5528T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5528 | chr4 | 17629326 | |||||
chr4:17629369
|
A | G | 1 | a0001c0001t0147 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5571A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5571 | chr4 | 17629369 | |||||
chr4:17629439
|
A | T | 2 | a0001c0001t0103a0001c0001t0104 | 2 | HG02258.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5641A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5641 | chr4 | 17629439 | |||||
chr4:17629452
|
C | T | 1 | a0001c0001t0122 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5654 | chr4 | 17629452 | |||||
chr4:17629537
|
C | T | 3 | a0001c0001t0009a0001c0001t0017a0001c0001t0085 | 9 | HG02622.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5739C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5739 | chr4 | 17629537 | |||||
chr4:17629630
|
T | C | 118 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(115): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*5832T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5832 | chr4 | 17629630 | |||||
chr4:17629654
|
T | C | 1 | a0001c0001t0152 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5856T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5856 | chr4 | 17629654 | |||||
chr4:17629834
|
A | G | 1 | a0001c0001t0071 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6036A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6036 | chr4 | 17629834 | |||||
chr4:17629855
|
A | G | 12 | a0001c0001t0030a0001c0001t0087a0001c0001t0088others(9): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6057A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6057 | chr4 | 17629855 | |||||
chr4:17629885
|
T | G | 1 | a0001c0001t0041 | 2 | HG01261.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6087T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6087 | chr4 | 17629885 | |||||
chr4:17629907
|
T | C | 3 | a0001c0001t0023a0001c0001t0062a0001c0001t0066 | 4 | HG02723.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6109T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6109 | chr4 | 17629907 | |||||
chr4:17630089
|
C | T | 1 | a0001c0001t0131 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6291C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6291 | chr4 | 17630089 | |||||
chr4:17630151
|
G | T | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6353G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6353 | chr4 | 17630151 | |||||
chr4:17630165
|
G | T | 6 | a0001c0001t0009a0001c0001t0017a0001c0001t0028others(3): Show | 14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6367G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6367 | chr4 | 17630165 | |||||
chr4:17630376
|
A | G | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6578A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6578 | chr4 | 17630376 | |||||
chr4:17630403
|
G | C | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6605G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6605 | chr4 | 17630403 | |||||
chr4:17630476
|
C | T | 1 | a0001c0001t0132 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6678C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6678 | chr4 | 17630476 | |||||
chr4:17630601
|
C | T | 8 | a0001c0001t0030a0001c0001t0092a0001c0001t0093others(5): Show | 9 | HG00544.hp1 HG02109.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6803C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6803 | chr4 | 17630601 | |||||
chr4:17630622
|
G | A | 1 | a0001c0001t0036 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6824G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6824 | chr4 | 17630622 | |||||
chr4:17630722
|
T | C | 2 | a0001c0001t0120a0001c0001t0123 | 2 | HG00642.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6924T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6924 | chr4 | 17630722 | |||||
chr4:17630779
|
C | CT | 7 | a0001c0001t0009a0001c0001t0017a0001c0001t0028others(4): Show | 16 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6993dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6994 | INFO_REALIGN_3_PRIME | chr4 | 17630779 | ||||
chr4:17630779
|
CT | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*6993delT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6993 | INFO_REALIGN_3_PRIME | chr4 | 17630779 | ||||
chr4:17630822
|
G | A | 1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7024G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7024 | chr4 | 17630822 | |||||
chr4:17630877
|
A | G | 4 | a0001c0001t0149a0001c0001t0150a0001c0001t0151others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7079A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7079 | chr4 | 17630877 | |||||
chr4:17630980
|
G | A | 2 | a0001c0001t0040a0001c0001t0135 | 3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7182G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7182 | chr4 | 17630980 | |||||
chr4:17631090
|
C | T | 1 | a0001c0002t0139 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7292C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7292 | chr4 | 17631090 | |||||
chr4:17631118
|
G | A | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7320G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7320 | chr4 | 17631118 | |||||
chr4:17631118
|
G | T | 7 | a0001c0001t0030a0001c0001t0092a0001c0001t0093others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7320G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7320 | chr4 | 17631118 | |||||
chr4:17631143
|
A | G | 5 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(2): Show | 7 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7345A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7345 | chr4 | 17631143 | |||||
chr4:17631209
|
TA | T | 5 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(2): Show | 7 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7412delA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7412 | chr4 | 17631209 | |||||
chr4:17631211
|
T | C | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*7413T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7413 | chr4 | 17631211 | |||||
chr4:17631212
|
A | T | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7414A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7414 | chr4 | 17631212 | |||||
chr4:17631214
|
A | T | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7416A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7416 | chr4 | 17631214 | |||||
chr4:17631215
|
T | C | 1 | a0001c0001t0126 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7417T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7417 | chr4 | 17631215 | |||||
chr4:17631216
|
A | T | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7418A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7418 | chr4 | 17631216 | |||||
chr4:17631218
|
A | T | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7420A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7420 | chr4 | 17631218 | |||||
chr4:17631220
|
A | T | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(74): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*7422A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7422 | chr4 | 17631220 | |||||
chr4:17631222
|
T | A | 2 | a0001c0001t0026a0001c0001t0154 | 3 | HG01361.hp2 HG02293.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7424T>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7424 | chr4 | 17631222 | |||||
chr4:17631227
|
T | C | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7429T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7429 | chr4 | 17631227 | |||||
chr4:17631331
|
CTAAT | C | 22 | a0001c0001t0030a0001c0001t0051a0001c0001t0087others(19): Show | 23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7536_*7539delATTA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7536 | INFO_REALIGN_3_PRIME | chr4 | 17631331 | ||||
chr4:17631365
|
G | C | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*7567G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7567 | chr4 | 17631365 | |||||
chr4:17631426
|
A | G | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*7628A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7628 | chr4 | 17631426 | |||||
chr4:17631454
|
G | A | 4 | a0001c0001t0012a0001c0001t0048a0001c0001t0049others(1): Show | 7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7656G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7656 | chr4 | 17631454 | |||||
chr4:17631585
|
C | A | 1 | a0001c0001t0063 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7787C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7787 | chr4 | 17631585 | |||||
chr4:17631596
|
T | TAATTCC | 5 | a0001c0001t0010a0001c0001t0034a0001c0001t0035others(2): Show | 11 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7804_*7809dupCAAT others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7810 | INFO_REALIGN_3_PRIME | chr4 | 17631596 | ||||
chr4:17631604
|
A | G | 22 | a0001c0001t0030a0001c0001t0051a0001c0001t0087others(19): Show | 23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7806A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7806 | chr4 | 17631604 | |||||
chr4:17631690
|
C | T | 1 | a0001c0001t0051 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7892C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7892 | chr4 | 17631690 | |||||
chr4:17631810
|
A | G | 1 | a0001c0001t0081 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8012A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8012 | chr4 | 17631810 | |||||
chr4:17631863
|
T | TG | 4 | a0001c0001t0149a0001c0001t0150a0001c0001t0151others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8066dupG | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8067 | INFO_REALIGN_3_PRIME | chr4 | 17631863 | ||||
chr4:17631907
|
C | A | 1 | a0001c0001t0045 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8109C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8109 | chr4 | 17631907 | |||||
chr4:17632042
|
AATTTTTT others(20): Show |
A | 1 | a0001c0001t0051 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8245_*8271delATTT others(23): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8245 | chr4 | 17632042 | |||||
chr4:17632043
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0153 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8280_*8289dupTTTT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8290 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0069 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8279_*8289dupTTTT others(7): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8290 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATT | A | 6 | a0001c0001t0017a0001c0001t0025a0001c0001t0061others(3): Show | 9 | HG02027.hp2 HG02698.hp1 HG03098.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8288_*8289delTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8288 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTT | A | 9 | a0001c0001t0009a0001c0001t0014a0001c0001t0023others(6): Show | 19 | HG00140.hp2 HG00544.hp2 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*8287_*8289delTTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8287 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTT | A | 7 | a0001c0001t0013a0001c0001t0029a0001c0001t0066others(4): Show | 11 | HG00738.hp1 HG01074.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8286_*8289delTTTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8286 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0035a0001c0001t0055 | 3 | HG00423.hp1 HG02055.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8280_*8289delTTTT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8280 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0010a0001c0001t0078a0001c0001t0103others(1): Show | 8 | HG00323.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8279_*8289delTTTT others(7): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8279 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0034 | 2 | HG02717.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8278_*8289delTTTT others(8): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8278 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0077 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8277_*8289delTTTT others(9): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8277 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0024a0001c0001t0081 | 3 | HG02132.hp1 HG02572.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8275_*8289delTTTT others(11): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8275 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0001t0022a0001c0001t0044 | 3 | HG03471.hp2 HG03486.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8273_*8289delTTTT others(13): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8273 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0021a0001c0001t0045a0001c0001t0047 | 4 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8272_*8289delTTTT others(14): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8272 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8271_*8289delTTTT others(15): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8271 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(13): Show |
A | 6 | a0001c0001t0012a0001c0001t0048a0001c0001t0049others(3): Show | 9 | HG00099.hp2 HG01255.hp2 HG01516.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8270_*8289delTTTT others(16): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8270 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(14): Show |
A | 2 | a0001c0001t0031a0001c0001t0076 | 3 | HG03491.hp2 HG03831.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8269_*8289delTTTT others(17): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(15): Show |
A | 5 | a0001c0001t0005a0001c0001t0018a0001c0001t0098others(2): Show | 14 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8268_*8289delTTTT others(18): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8268 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(16): Show |
A | 2 | a0001c0001t0075a0001c0001t0101 | 2 | HG04228.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8267_*8289delTTTT others(19): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8267 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(18): Show |
A | 1 | a0001c0001t0028 | 2 | HG02818.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8265_*8289delTTTT others(21): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8265 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(19): Show |
A | 5 | a0001c0001t0087a0001c0001t0088a0001c0001t0089others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8264_*8289delTTTT others(22): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8264 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(20): Show |
A | 17 | a0001c0001t0030a0001c0001t0050a0001c0001t0092others(14): Show | 18 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8263_*8289delTTTT others(23): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8263 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(21): Show |
A | 5 | a0001c0001t0039a0001c0001t0121a0001c0001t0145others(2): Show | 6 | HG01516.hp2 HG02257.hp1 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8262_*8289delTTTT others(24): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8262 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(22): Show |
A | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*8261_*8289delTTTT others(25): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8261 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632043
|
ATTTTTTT others(23): Show |
A | 1 | a0001c0001t0128 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8260_*8289delTTTT others(26): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8260 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | ||||
chr4:17632103
|
C | T | 1 | a0001c0001t0087 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8305C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8305 | chr4 | 17632103 | |||||
chr4:17632160
|
T | TGCCTCCT others(18): Show |
1 | a0001c0001t0048 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8363_*8387dupGCCT others(21): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8388 | INFO_REALIGN_3_PRIME | chr4 | 17632160 | ||||
chr4:17632187
|
G | A | 7 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(4): Show | 9 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8389G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8389 | chr4 | 17632187 | |||||
chr4:17632284
|
A | G | 2 | a0001c0001t0059a0001c0001t0065 | 2 | HG00609.hp2 HG00673.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8486A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8486 | chr4 | 17632284 | |||||
chr4:17632330
|
C | G | 1 | a0001c0001t0043 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8532C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8532 | chr4 | 17632330 | |||||
chr4:17632590
|
A | G | 159 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(156): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*8792A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8792 | chr4 | 17632590 | |||||
chr4:17632632
|
G | A | 92 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*8834G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8834 | chr4 | 17632632 | |||||
chr4:17632633
|
C | CAA | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*8841_*8842dupAA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8843 | INFO_REALIGN_3_PRIME | chr4 | 17632633 | ||||
chr4:17632690
|
A | ACC | 3 | a0001c0001t0012a0001c0001t0049a0001c0001t0050 | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8893_*8894dupCC | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8895 | INFO_REALIGN_3_PRIME | chr4 | 17632690 | ||||
chr4:17632737
|
C | T | 22 | a0001c0001t0030a0001c0001t0051a0001c0001t0087others(19): Show | 23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*8939C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8939 | chr4 | 17632737 | |||||
chr4:17632819
|
G | T | 92 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*9021G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9021 | chr4 | 17632819 | |||||
chr4:17632847
|
T | C | 1 | a0001c0001t0096 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9049T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9049 | chr4 | 17632847 | |||||
chr4:17633016
|
G | T | 2 | a0001c0001t0046a0001c0001t0155 | 2 | HG03098.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9218G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9218 | chr4 | 17633016 | |||||
chr4:17633048
|
G | A | 22 | a0001c0001t0030a0001c0001t0051a0001c0001t0087others(19): Show | 23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*9250G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9250 | chr4 | 17633048 | |||||
chr4:17633142
|
G | A | 2 | a0001c0001t0129a0001c0001t0130 | 2 | NA18982.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9344G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9344 | chr4 | 17633142 | |||||
chr4:17633218
|
G | A | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9420G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9420 | chr4 | 17633218 | |||||
chr4:17633245
|
A | G | 1 | a0001c0001t0152 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9447A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9447 | chr4 | 17633245 | |||||
chr4:17633321
|
C | T | 1 | a0001c0001t0149 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9523C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9523 | chr4 | 17633321 | |||||
chr4:17633363
|
G | A | 1 | a0001c0001t0151 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9565G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9565 | chr4 | 17633363 | |||||
chr4:17633713
|
G | A | 1 | a0001c0001t0026 | 2 | HG01361.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9915G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9915 | chr4 | 17633713 | |||||
chr4:17633765
|
G | T | 1 | a0001c0001t0051 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9967G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9967 | chr4 | 17633765 | |||||
chr4:17633886
|
T | C | 1 | a0001c0001t0088 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10088T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10088 | chr4 | 17633886 | |||||
chr4:17633933
|
CAAAAT | C | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*10139_*10143delAT others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10139 | INFO_REALIGN_3_PRIME | chr4 | 17633933 | ||||
chr4:17633987
|
C | T | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0044others(3): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10189C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10189 | chr4 | 17633987 | |||||
chr4:17633988
|
G | A | 1 | a0001c0001t0133 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10190G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10190 | chr4 | 17633988 | |||||
chr4:17634028
|
T | C | 7 | a0001c0001t0030a0001c0001t0092a0001c0001t0093others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10230T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10230 | chr4 | 17634028 | |||||
chr4:17634065
|
A | G | 1 | a0001c0001t0136 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10267A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10267 | chr4 | 17634065 | |||||
chr4:17634080
|
G | A | 2 | a0001c0001t0040a0001c0001t0135 | 3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10282G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10282 | chr4 | 17634080 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:17614883
|
G | T | 1 | a0001c0001t0007g0106 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.159+70G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17614883 | ||||||
chr4:17614914
|
C | T | 13 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0087g0103others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+101C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17614914 | ||||||
chr4:17615054
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.159+241A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615054 | ||||||
chr4:17615263
|
G | C | 1 | a0001c0001t0126g0037 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.159+450G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615263 | ||||||
chr4:17615393
|
G | A | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.159+580G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615393 | ||||||
chr4:17615402
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.159+589G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615402 | ||||||
chr4:17615488
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.159+675T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615488 | ||||||
chr4:17615563
|
G | A | 1 | a0001c0001t0150g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159+750G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615563 | ||||||
chr4:17615565
|
A | G | 1 | a0001c0001t0048g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+752A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615565 | ||||||
chr4:17615585
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.159+772G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615585 | ||||||
chr4:17615638
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.159+825T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615638 | ||||||
chr4:17615765
|
G | A | 11 | a0001c0001t0005g0029a0001c0001t0005g0074a0001c0001t0021g0066others(8): Show | 11 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+952G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615765 | ||||||
chr4:17615850
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(226): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.159+1037C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615850 | ||||||
chr4:17615863
|
GTATT | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0021a0001c0001t0005g0029others(21): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.159+1051_159+1054d others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615863 | ||||||
chr4:17615867
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.159+1054T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615867 | ||||||
chr4:17615868
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0021a0001c0001t0005g0029others(21): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.159+1055G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615868 | ||||||
chr4:17615945
|
C | T | 1 | a0001c0001t0021g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159+1132C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615945 | ||||||
chr4:17615994
|
T | C | 1 | a0001c0001t0006g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.159+1181T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615994 | ||||||
chr4:17615999
|
C | T | 9 | a0001c0001t0087g0103a0001c0001t0088g0105a0001c0001t0089g0036others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+1186C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615999 | ||||||
chr4:17616086
|
G | A | 1 | a0001c0001t0116g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.159+1273G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616086 | ||||||
chr4:17616091
|
G | T | 1 | a0001c0001t0048g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+1278G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616091 | ||||||
chr4:17616146
|
A | G | 12 | a0001c0001t0087g0103a0001c0001t0088g0105a0001c0001t0089g0036others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1333A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616146 | ||||||
chr4:17616164
|
C | T | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.159+1351C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616164 | ||||||
chr4:17616338
|
G | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.159+1525G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616338 | ||||||
chr4:17616386
|
G | C | 1 | a0001c0001t0150g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159+1573G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616386 | ||||||
chr4:17616401
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.159+1588G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616401 | ||||||
chr4:17616426
|
A | G | 48 | a0001c0001t0006g0002a0001c0001t0006g0081a0001c0001t0006g0087others(45): Show | 56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.159+1613A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616426 | ||||||
chr4:17616545
|
C | T | 2 | a0001c0001t0147g0023a0001c0001t0148g0023 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.159+1732C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616545 | ||||||
chr4:17616553
|
C | G | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+1740C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616553 | ||||||
chr4:17616821
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.159+2008A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616821 | ||||||
chr4:17616883
|
T | G | 5 | a0001c0001t0087g0103a0001c0001t0088g0105a0001c0001t0089g0036others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+2070T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616883 | ||||||
chr4:17616901
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.159+2088G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616901 | ||||||
chr4:17616950
|
G | A | 1 | a0001c0001t0049g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.159+2137G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616950 | ||||||
chr4:17617034
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.159+2221G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617034 | ||||||
chr4:17617088
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.159+2275A>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617088 | ||||||
chr4:17617090
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.159+2277G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617090 | ||||||
chr4:17617341
|
A | G | 1 | a0001c0001t0048g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+2528A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617341 | ||||||
chr4:17617379
|
C | G | 1 | a0001c0001t0051g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.160-2522C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617379 | ||||||
chr4:17617553
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0002g0014a0001c0001t0019g0014 | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-2348A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617553 | ||||||
chr4:17617561
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.160-2340A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617561 | ||||||
chr4:17617632
|
T | C | 1 | a0001c0001t0069g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.160-2269T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617632 | ||||||
chr4:17617634
|
C | T | 1 | a0001c0001t0037g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160-2267C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617634 | ||||||
chr4:17617642
|
C | T | 2 | a0001c0001t0013g0035a0001c0001t0014g0035 | 2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.160-2259C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617642 | ||||||
chr4:17617704
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.160-2197C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617704 | ||||||
chr4:17617759
|
T | G | 7 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-2142T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617759 | ||||||
chr4:17617764
|
G | C | 7 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-2137G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617764 | ||||||
chr4:17617806
|
C | T | 1 | a0001c0001t0149g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.160-2095C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617806 | ||||||
chr4:17617883
|
G | A | 2 | a0001c0001t0058g0030a0001c0001t0060g0030 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.160-2018G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617883 | ||||||
chr4:17617998
|
T | C | 1 | a0001c0001t0095g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.160-1903T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617998 | ||||||
chr4:17618013
|
C | CT | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.160-1872dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618013 | |||||
chr4:17618013
|
C | CTT | 8 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0007g0011others(5): Show | 8 | HG00438.hp1 HG00438.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-1873_160-1872d others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618013 | |||||
chr4:17618013
|
CTT | C | 6 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-1873_160-1872d others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618013 | |||||
chr4:17618016
|
T | TC | 9 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0087g0103others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-1885_160-1884i others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618016 | ||||||
chr4:17618068
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.160-1833A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618068 | ||||||
chr4:17618075
|
G | A | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.160-1826G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618075 | ||||||
chr4:17618101
|
TC | T | 4 | a0001c0001t0012g0022a0001c0001t0012g0033a0001c0001t0049g0082others(1): Show | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-1798delC | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618101 | |||||
chr4:17618208
|
C | A | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1693C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618208 | ||||||
chr4:17618213
|
T | C | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1688T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618213 | ||||||
chr4:17618312
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160-1589T>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618312 | ||||||
chr4:17618324
|
G | T | 8 | a0001c0001t0009g0003a0001c0001t0009g0083a0001c0001t0017g0003others(5): Show | 14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-1577G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618324 | ||||||
chr4:17618367
|
A | T | 8 | a0001c0001t0009g0003a0001c0001t0009g0083a0001c0001t0017g0003others(5): Show | 14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-1534A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618367 | ||||||
chr4:17618385
|
C | G | 1 | a0001c0001t0002g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.160-1516C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618385 | ||||||
chr4:17618443
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.160-1458A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618443 | ||||||
chr4:17618476
|
A | G | 4 | a0001c0001t0025g0095a0001c0002t0020g0013a0001c0002t0139g0013others(1): Show | 5 | HG02970.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-1425A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618476 | ||||||
chr4:17618542
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.160-1359A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618542 | ||||||
chr4:17618548
|
G | A | 1 | a0001c0001t0074g0086 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.160-1353G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618548 | ||||||
chr4:17618619
|
C | T | 8 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0092g0016others(5): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1282C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618619 | ||||||
chr4:17618663
|
C | T | 1 | a0001c0001t0152g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.160-1238C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618663 | ||||||
chr4:17618718
|
G | A | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.160-1183G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618718 | ||||||
chr4:17618734
|
TGA | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.160-1166_160-1165d others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618734 | ||||||
chr4:17618739
|
TCGTG | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.160-1161_160-1158d others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618739 | ||||||
chr4:17618747
|
CTGCCTTC others(10): Show |
C | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.160-1152_160-1136d others(19): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618747 | |||||
chr4:17618775
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0003g0007 | 8 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1126G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618775 | ||||||
chr4:17618945
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.160-956G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618945 | ||||||
chr4:17619045
|
T | C | 1 | a0001c0001t0087g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160-856T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619045 | ||||||
chr4:17619067
|
C | T | 7 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0092g0016others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-834C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619067 | ||||||
chr4:17619086
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.160-815C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619086 | ||||||
chr4:17619110
|
C | G | 1 | a0001c0001t0108g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.160-791C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619110 | ||||||
chr4:17619136
|
A | G | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-765A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619136 | ||||||
chr4:17619227
|
A | C | 2 | a0001c0001t0032g0015a0001c0001t0033g0015 | 4 | HG01109.hp1 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-674A>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619227 | ||||||
chr4:17619248
|
G | T | 1 | a0001c0001t0013g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.160-653G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619248 | ||||||
chr4:17619436
|
G | T | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.160-465G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619436 | ||||||
chr4:17619508
|
G | C | 1 | a0001c0001t0006g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-393G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619508 | ||||||
chr4:17619687
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.160-214G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619687 | ||||||
chr4:17619702
|
C | T | 2 | a0001c0001t0093g0102a0001c0001t0094g0101 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.160-199C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619702 | ||||||
chr4:17619759
|
G | A | 4 | a0001c0001t0149g0073a0001c0001t0150g0064a0001c0001t0151g0071others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-142G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619759 | ||||||
chr4:17619760
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.160-141C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619760 | ||||||
chr4:17619986
|
T | C | 4 | a0001c0001t0012g0022a0001c0001t0012g0033a0001c0001t0049g0082others(1): Show | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+19T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17619986 | ||||||
chr4:17620038
|
C | A | 1 | a0001c0001t0094g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.226+71C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620038 | ||||||
chr4:17620141
|
G | A | 1 | a0001c0001t0046g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226+174G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620141 | ||||||
chr4:17620154
|
T | TAACGAAT others(327): Show |
1 | a0001c0001t0095g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226+201_226+202ins others(334): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620154 | |||||
chr4:17620190
|
C | G | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+223C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620190 | ||||||
chr4:17620337
|
C | T | 1 | a0001c0001t0046g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226+370C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620337 | ||||||
chr4:17620354
|
G | GT | 31 | a0001c0001t0009g0003a0001c0001t0013g0093a0001c0001t0017g0003others(28): Show | 37 | HG01123.hp1 HG01175.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.226+402dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620354 | |||||
chr4:17620354
|
G | GTT | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(100): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.226+401_226+402dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620354 | |||||
chr4:17620354
|
G | GTTT | 19 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0002g0006others(16): Show | 20 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.226+400_226+402dup others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620354 | |||||
chr4:17620441
|
C | G | 8 | a0001c0001t0009g0003a0001c0001t0009g0083a0001c0001t0017g0003others(5): Show | 14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.226+474C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620441 | ||||||
chr4:17620538
|
G | A | 1 | a0001c0001t0061g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.226+571G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620538 | ||||||
chr4:17620613
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0132g0044 | 3 | HG02717.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.226+646G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620613 | ||||||
chr4:17620622
|
C | T | 2 | a0001c0001t0149g0073a0001c0001t0150g0064 | 2 | HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.226+655C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620622 | ||||||
chr4:17620689
|
TCTC | T | 5 | a0001c0001t0022g0020a0001c0001t0022g0069a0001c0001t0045g0020others(2): Show | 5 | HG02630.hp1 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+723_226+725del others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620689 | ||||||
chr4:17620690
|
C | T | 3 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0044g0067 | 3 | HG02451.hp1 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.226+723C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620690 | ||||||
chr4:17620692
|
C | CT | 5 | a0001c0001t0012g0022a0001c0001t0012g0033a0001c0001t0026g0092others(2): Show | 7 | HG00099.hp2 HG01361.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+746dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | |||||
chr4:17620692
|
C | CTT | 10 | a0001c0001t0010g0009a0001c0001t0010g0076a0001c0001t0032g0015others(7): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.226+745_226+746dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | |||||
chr4:17620692
|
C | CTTTTT | 9 | a0001c0001t0005g0005a0001c0001t0005g0074a0001c0001t0018g0005others(6): Show | 13 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+742_226+746dup others(5): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | |||||
chr4:17620692
|
CTT | C | 14 | a0001c0001t0001g0004a0001c0001t0002g0004a0001c0001t0002g0053others(11): Show | 18 | HG01106.hp2 HG01243.hp2 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+745_226+746del others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | |||||
chr4:17620692
|
CTTT | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.226+744_226+746del others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | |||||
chr4:17620695
|
T | C | 5 | a0001c0001t0022g0020a0001c0001t0022g0069a0001c0001t0045g0020others(2): Show | 5 | HG02630.hp1 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+728T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620695 | ||||||
chr4:17620713
|
T | G | 1 | a0001c0001t0136g0045 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.226+746T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620713 | ||||||
chr4:17620732
|
C | G | 1 | a0001c0001t0011g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+765C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620732 | ||||||
chr4:17620758
|
A | G | 4 | a0001c0001t0149g0073a0001c0001t0150g0064a0001c0001t0151g0071others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+791A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620758 | ||||||
chr4:17620947
|
G | A | 13 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0087g0103others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.227-640G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620947 | ||||||
chr4:17621018
|
G | GT | 8 | a0001c0001t0010g0009a0001c0001t0010g0075a0001c0001t0018g0077others(5): Show | 11 | HG01123.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.227-554dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17621018 | |||||
chr4:17621018
|
G | GTT | 21 | a0001c0001t0002g0053a0001c0001t0010g0076a0001c0001t0030g0016others(18): Show | 21 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-555_227-554dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17621018 | |||||
chr4:17621018
|
G | GTTT | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.227-556_227-554dup others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17621018 | |||||
chr4:17621038
|
C | T | 1 | a0001c0001t0031g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.227-549C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621038 | ||||||
chr4:17621134
|
C | T | 1 | a0001c0001t0028g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.227-453C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621134 | ||||||
chr4:17621170
|
C | T | 1 | a0001c0001t0012g0033 | 2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.227-417C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621170 | ||||||
chr4:17621203
|
G | A | 4 | a0001c0001t0012g0022a0001c0001t0012g0033a0001c0001t0049g0082others(1): Show | 6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-384G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621203 | ||||||
chr4:17621263
|
C | T | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-324C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621263 | ||||||
chr4:17621287
|
C | T | 4 | a0001c0001t0013g0093a0001c0001t0027g0034a0001c0001t0068g0090others(1): Show | 4 | HG00735.hp2 HG00738.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-300C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621287 | ||||||
chr4:17621306
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.227-281C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621306 | ||||||
chr4:17621369
|
T | C | 1 | a0001c0001t0004g0048 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.227-218T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621369 | ||||||
chr4:17621391
|
G | A | 4 | a0001c0001t0149g0073a0001c0001t0150g0064a0001c0001t0151g0071others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-196G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621391 | ||||||
chr4:17621401
|
T | C | 12 | a0001c0001t0009g0003a0001c0001t0009g0083a0001c0001t0017g0003others(9): Show | 18 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.227-186T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621401 | ||||||
chr4:17621473
|
C | T | 3 | a0001c0002t0020g0013a0001c0002t0139g0013a0001c0004t0020g0013 | 4 | HG02970.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-114C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621473 | ||||||
chr4:17621557
|
T | C | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.227-30T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621557 | ||||||
chr4:17621718
|
C | G | 4 | a0001c0001t0149g0073a0001c0001t0150g0064a0001c0001t0151g0071others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+19C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17621718 | ||||||
chr4:17621764
|
G | T | 1 | a0001c0001t0048g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+65G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17621764 | ||||||
chr4:17621930
|
G | A | 1 | a0001c0001t0048g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+231G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17621930 | ||||||
chr4:17622046
|
A | G | 8 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0092g0016others(5): Show | 8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+347A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622046 | ||||||
chr4:17622082
|
A | G | 2 | a0001c0001t0032g0015a0001c0001t0033g0015 | 4 | HG01109.hp1 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+383A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622082 | ||||||
chr4:17622174
|
T | C | 3 | a0001c0001t0040g0025a0001c0001t0040g0058a0001c0001t0135g0025 | 3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.339+475T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622174 | ||||||
chr4:17622285
|
A | G | 11 | a0001c0001t0002g0008a0001c0001t0002g0054a0001c0001t0003g0008others(8): Show | 15 | HG00099.hp2 HG00280.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.339+586A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622285 | ||||||
chr4:17622377
|
T | G | 4 | a0001c0001t0155g0027a0001c0001t0156g0027a0001c0001t0157g0028others(1): Show | 4 | HG02451.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+678T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622377 | ||||||
chr4:17622411
|
C | T | 8 | a0001c0001t0021g0066a0001c0001t0021g0070a0001c0001t0022g0020others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+712C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622411 | ||||||
chr4:17622426
|
G | C | 1 | a0001c0001t0015g0049 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.339+727G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622426 | ||||||
chr4:17622472
|
A | T | 1 | a0001c0001t0004g0018 | 3 | HG01167.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.339+773A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622472 | ||||||
chr4:17622554
|
TGATA | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0021a0001c0001t0005g0029others(21): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+859_339+862del others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17622554 | |||||
chr4:17622623
|
G | A | 5 | a0001c0001t0087g0103a0001c0001t0088g0105a0001c0001t0089g0036others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+924G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622623 | ||||||
chr4:17622829
|
C | T | 15 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0092g0016others(12): Show | 15 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.340-772C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622829 | ||||||
chr4:17622863
|
G | A | 13 | a0001c0001t0030g0016a0001c0001t0030g0100a0001c0001t0092g0016others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-738G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622863 | ||||||
chr4:17622869
|
T | C | 4 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-732T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622869 | ||||||
chr4:17622884
|
C | A | 5 | a0001c0001t0111g0012a0001c0001t0112g0012a0001c0001t0113g0012others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-717C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622884 | ||||||
chr4:17622926
|
T | C | 1 | a0001c0001t0152g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.340-675T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622926 | ||||||
chr4:17622943
|
C | T | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.340-658C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622943 | ||||||
chr4:17622978
|
G | A | 1 | a0001c0001t0150g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.340-623G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622978 | ||||||
chr4:17623039
|
C | T | 1 | a0001c0001t0061g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.340-562C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623039 | ||||||
chr4:17623145
|
A | G | 5 | a0001c0001t0087g0103a0001c0001t0088g0105a0001c0001t0089g0036others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-456A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623145 | ||||||
chr4:17623146
|
ATCCTAGC others(10): Show |
A | 5 | a0001c0001t0087g0103a0001c0001t0088g0105a0001c0001t0089g0036others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-454_340-438del others(17): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623146 | ||||||
chr4:17623220
|
G | T | 1 | a0001c0001t0046g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.340-381G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623220 | ||||||
chr4:17623227
|
C | T | 1 | a0001c0001t0146g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.340-374C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623227 | ||||||
chr4:17623264
|
G | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-337G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623264 | ||||||
chr4:17623267
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.340-334G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623267 | ||||||
chr4:17623268
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.340-333G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623268 | ||||||
chr4:17623349
|
C | T | 3 | a0001c0001t0146g0038a0001c0001t0147g0023a0001c0001t0148g0023 | 3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.340-252C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623349 | ||||||
chr4:17623398
|
C | CA | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(129): Show | 199 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.340-186dupA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17623398 | |||||
chr4:17623398
|
C | CAA | 11 | a0001c0001t0001g0059a0001c0001t0002g0017a0001c0001t0003g0017others(8): Show | 13 | HG00099.hp1 HG00099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-187_340-186dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17623398 | |||||
chr4:17623398
|
CA | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0021a0001c0001t0005g0029others(21): Show | 34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.340-186delA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17623398 | |||||
chr4:17623431
|
T | C | 1 | a0001c0001t0001g0024 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.340-170T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623431 | ||||||
chr4:17623580
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0003g0010a0001c0001t0106g0010others(1): Show | 5 | HG02083.hp2 NA18982.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-21G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623580 | ||||||
chr4:17623586
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.340-15G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623586 |