Variant report
Variant | rs10028250 |
---|---|
Chromosome Location | chr4:110311943-110311944 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10000545 | 0.86[JPT][hapmap] |
rs10002595 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs10016533 | 1.00[MEX][hapmap] |
rs10155127 | 0.86[JPT][hapmap] |
rs10155246 | 0.92[CEU][hapmap] |
rs11098033 | 0.90[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes] |
rs11098035 | 0.90[CHD][hapmap];0.86[JPT][hapmap] |
rs11929713 | 0.84[CHD][hapmap];0.85[JPT][hapmap] |
rs11930655 | 0.84[JPT][hapmap] |
rs11933172 | 0.93[CEU][hapmap];0.90[CHD][hapmap];0.83[GIH][hapmap] |
rs11934486 | 0.81[ASN][1000 genomes] |
rs11935440 | 0.81[ASN][1000 genomes] |
rs11935629 | 0.81[ASN][1000 genomes] |
rs11938593 | 0.81[ASN][1000 genomes] |
rs11939924 | 0.91[ASN][1000 genomes] |
rs11942140 | 0.88[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs11942291 | 1.00[JPT][hapmap] |
rs11942858 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs11942928 | 0.81[ASN][1000 genomes] |
rs11943384 | 0.85[JPT][hapmap];0.81[ASN][1000 genomes] |
rs11943430 | 0.86[JPT][hapmap];0.81[ASN][1000 genomes] |
rs11944375 | 0.81[ASN][1000 genomes] |
rs11944427 | 0.81[ASN][1000 genomes] |
rs11944659 | 0.81[ASN][1000 genomes] |
rs12639832 | 0.81[ASN][1000 genomes] |
rs12640049 | 0.88[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs12643055 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs12644055 | 0.81[ASN][1000 genomes] |
rs12647695 | 0.81[ASN][1000 genomes] |
rs12648138 | 0.86[JPT][hapmap] |
rs12648965 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs12650654 | 0.90[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes] |
rs12650873 | 0.81[ASN][1000 genomes] |
rs13103034 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs13113384 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs13119700 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs13123618 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs13128445 | 0.85[MEX][hapmap] |
rs13138833 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs13142698 | 0.90[CHD][hapmap];1.00[MEX][hapmap] |
rs13143825 | 0.86[JPT][hapmap] |
rs13145066 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs1509314 | 1.00[JPT][hapmap] |
rs1509315 | 0.86[JPT][hapmap] |
rs17040410 | 0.81[ASN][1000 genomes] |
rs17040436 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs17040439 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs17040461 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs17585970 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs17619262 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs2346014 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs28585579 | 0.85[ASN][1000 genomes] |
rs28628718 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs28681408 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs61553525 | 0.81[ASN][1000 genomes] |
rs6533426 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs6533429 | 0.81[ASN][1000 genomes] |
rs6533434 | 1.00[MEX][hapmap] |
rs6815455 | 0.86[JPT][hapmap] |
rs6818911 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs6825928 | 0.93[CEU][hapmap];0.88[MEX][hapmap] |
rs6835683 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs6841133 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs6841198 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs6841222 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs6848452 | 0.83[AMR][1000 genomes] |
rs6851517 | 0.81[ASN][1000 genomes] |
rs6856291 | 0.86[JPT][hapmap] |
rs7436583 | 0.90[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs7436745 | 0.90[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes] |
rs7440371 | 0.81[ASN][1000 genomes] |
rs7440570 | 0.86[JPT][hapmap] |
rs7673595 | 0.93[CEU][hapmap] |
rs7675344 | 0.93[CEU][hapmap] |
rs7675602 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs7684744 | 0.95[ASN][1000 genomes] |
rs7685787 | 0.85[ASN][1000 genomes] |
rs7687245 | 0.86[JPT][hapmap] |
rs7695754 | 0.91[CEU][hapmap] |
rs876464 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs9985632 | 0.85[CHD][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap] |
rs9985964 | 0.86[JPT][hapmap] |
rs9993228 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs9994676 | 0.85[CHD][hapmap];0.86[JPT][hapmap] |
rs9996165 | 0.92[CEU][hapmap] |
rs9996432 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs9999570 | 0.85[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv461613 | chr4:109922064-110593460 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
2 | nsv595129 | chr4:109922064-110593460 | Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
3 | esv1799708 | chr4:110309234-110333106 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:110306600-110316400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr4:110310600-110316800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr4:110310800-110317000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
4 | chr4:110310800-110318800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
5 | chr4:110311200-110317000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
6 | chr4:110311200-110327800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
7 | chr4:110311600-110312000 | Enhancers | GM12878-XiMat | blood |
8 | chr4:110311600-110331400 | Weak transcription | HSMMtube | muscle |
9 | chr4:110311800-110312200 | Enhancers | Fetal Muscle Leg | muscle |