Variant report
Variant | rs6532903 |
---|---|
Chromosome Location | chr4:101754754-101754755 |
allele | A/G |
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] |
---|---|
rs10008442 | 0.94[ASN][1000 genomes] |
rs10013582 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10013744 | 1.00[ASN][1000 genomes] |
rs10516476 | 1.00[ASN][1000 genomes] |
rs13102244 | 0.91[EUR][1000 genomes] |
rs13102501 | 0.94[ASN][1000 genomes] |
rs13102608 | 0.90[EUR][1000 genomes] |
rs13104590 | 0.90[EUR][1000 genomes] |
rs13104901 | 0.91[EUR][1000 genomes] |
rs13107645 | 0.91[EUR][1000 genomes] |
rs13109446 | 0.91[EUR][1000 genomes] |
rs13110542 | 0.91[EUR][1000 genomes] |
rs13110644 | 0.91[EUR][1000 genomes] |
rs13111905 | 0.91[EUR][1000 genomes] |
rs13116153 | 0.91[EUR][1000 genomes] |
rs13117474 | 0.89[CEU][hapmap] |
rs13118441 | 0.94[ASN][1000 genomes] |
rs13120027 | 0.90[EUR][1000 genomes] |
rs13121245 | 0.91[EUR][1000 genomes] |
rs13121438 | 0.91[EUR][1000 genomes] |
rs13122395 | 1.00[ASN][1000 genomes] |
rs13122599 | 0.91[EUR][1000 genomes] |
rs13123162 | 0.91[EUR][1000 genomes] |
rs13129721 | 0.91[EUR][1000 genomes] |
rs13130074 | 0.91[EUR][1000 genomes] |
rs13130138 | 0.94[ASN][1000 genomes] |
rs13131485 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13132028 | 0.90[EUR][1000 genomes] |
rs13138965 | 0.90[EUR][1000 genomes] |
rs13150288 | 0.91[EUR][1000 genomes] |
rs1390930 | 1.00[ASN][1000 genomes] |
rs1390931 | 0.91[EUR][1000 genomes] |
rs1390932 | 0.91[EUR][1000 genomes] |
rs1390933 | 1.00[ASN][1000 genomes] |
rs1390934 | 1.00[ASN][1000 genomes] |
rs1390936 | 0.89[CEU][hapmap];0.90[EUR][1000 genomes] |
rs1566119 | 0.90[EUR][1000 genomes] |
rs17030481 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17030500 | 1.00[ASN][1000 genomes] |
rs17030502 | 1.00[ASN][1000 genomes] |
rs17030525 | 0.90[EUR][1000 genomes] |
rs17227226 | 0.91[EUR][1000 genomes] |
rs17635262 | 0.88[CEU][hapmap] |
rs17635286 | 0.88[CEU][hapmap] |
rs17813352 | 0.91[EUR][1000 genomes] |
rs17813556 | 1.00[CEU][hapmap];0.91[EUR][1000 genomes] |
rs17813598 | 1.00[CEU][hapmap];0.91[EUR][1000 genomes] |
rs17813670 | 0.91[EUR][1000 genomes] |
rs17813694 | 0.91[EUR][1000 genomes] |
rs28444682 | 0.90[EUR][1000 genomes] |
rs28701141 | 1.00[ASN][1000 genomes] |
rs2903222 | 0.91[EUR][1000 genomes] |
rs34080291 | 0.91[EUR][1000 genomes] |
rs34103148 | 0.90[EUR][1000 genomes] |
rs34126461 | 0.91[EUR][1000 genomes] |
rs34394941 | 0.90[EUR][1000 genomes] |
rs34674329 | 0.90[EUR][1000 genomes] |
rs34716852 | 0.91[EUR][1000 genomes] |
rs34742412 | 1.00[CEU][hapmap];0.81[TSI][hapmap];0.90[EUR][1000 genomes] |
rs34754564 | 0.91[EUR][1000 genomes] |
rs34802397 | 0.91[EUR][1000 genomes] |
rs34810105 | 0.91[EUR][1000 genomes] |
rs34833700 | 0.91[EUR][1000 genomes] |
rs34839174 | 0.91[EUR][1000 genomes] |
rs34885747 | 0.90[EUR][1000 genomes] |
rs34891917 | 0.91[EUR][1000 genomes] |
rs34920876 | 0.91[EUR][1000 genomes] |
rs35024886 | 0.91[EUR][1000 genomes] |
rs35150863 | 0.91[EUR][1000 genomes] |
rs35170503 | 0.91[EUR][1000 genomes] |
rs35481231 | 0.91[EUR][1000 genomes] |
rs35540482 | 1.00[ASN][1000 genomes] |
rs35554164 | 0.91[EUR][1000 genomes] |
rs35564595 | 0.91[EUR][1000 genomes] |
rs35629108 | 0.91[EUR][1000 genomes] |
rs35664627 | 0.91[EUR][1000 genomes] |
rs35795105 | 0.88[EUR][1000 genomes] |
rs35807447 | 1.00[ASN][1000 genomes] |
rs35863364 | 0.91[EUR][1000 genomes] |
rs35969070 | 0.90[EUR][1000 genomes] |
rs36091097 | 0.91[EUR][1000 genomes] |
rs58690640 | 1.00[ASN][1000 genomes] |
rs58926631 | 1.00[ASN][1000 genomes] |
rs62305818 | 0.90[EUR][1000 genomes] |
rs62305826 | 0.91[EUR][1000 genomes] |
rs62305828 | 0.91[EUR][1000 genomes] |
rs62305832 | 0.91[EUR][1000 genomes] |
rs62305833 | 0.91[EUR][1000 genomes] |
rs62305834 | 0.91[EUR][1000 genomes] |
rs62305843 | 0.91[EUR][1000 genomes] |
rs62307671 | 0.91[EUR][1000 genomes] |
rs62307673 | 0.90[EUR][1000 genomes] |
rs62307674 | 0.91[EUR][1000 genomes] |
rs62307677 | 0.91[EUR][1000 genomes] |
rs62307678 | 0.91[EUR][1000 genomes] |
rs62307679 | 0.91[EUR][1000 genomes] |
rs62307680 | 0.91[EUR][1000 genomes] |
rs62307682 | 0.90[EUR][1000 genomes] |
rs62307685 | 0.90[EUR][1000 genomes] |
rs62307719 | 0.90[EUR][1000 genomes] |
rs62307725 | 0.90[EUR][1000 genomes] |
rs6419156 | 1.00[ASN][1000 genomes] |
rs6831914 | 1.00[ASN][1000 genomes] |
rs6835722 | 0.90[EUR][1000 genomes] |
rs6840437 | 0.90[EUR][1000 genomes] |
rs6840973 | 0.87[EUR][1000 genomes] |
rs71600272 | 0.90[EUR][1000 genomes] |
rs7434953 | 0.91[EUR][1000 genomes] |
rs7437932 | 0.91[EUR][1000 genomes] |
rs7441213 | 0.91[EUR][1000 genomes] |
rs7441263 | 0.88[EUR][1000 genomes] |
rs7441325 | 0.91[EUR][1000 genomes] |
rs7655125 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.94[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7667871 | 0.90[EUR][1000 genomes] |
rs7676752 | 0.90[EUR][1000 genomes] |
rs7681227 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7686000 | 0.90[EUR][1000 genomes] |
rs7689536 | 1.00[ASN][1000 genomes] |
rs7696663 | 0.90[EUR][1000 genomes] |
rs931622 | 0.91[EUR][1000 genomes] |
rs9991123 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv931418 | chr4:101500167-102443207 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:101745400-101758800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
2 | chr4:101753000-101758000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
3 | chr4:101754200-101755000 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |