Variant report
Variant | rs9489153 |
---|---|
Chromosome Location | chr6:117736103-117736104 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:117732882..117736812-chr6:117738044..117741372,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10046392 | 0.88[AFR][1000 genomes] |
rs10484302 | 0.92[ASN][1000 genomes] |
rs11153660 | 0.85[AFR][1000 genomes] |
rs11756910 | 0.86[AFR][1000 genomes] |
rs12332806 | 0.88[AFR][1000 genomes] |
rs12332810 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13196657 | 0.92[ASN][1000 genomes] |
rs13197031 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13199989 | 0.92[ASN][1000 genomes] |
rs13202073 | 0.84[ASN][1000 genomes] |
rs13202720 | 0.92[ASN][1000 genomes] |
rs13205893 | 0.84[ASN][1000 genomes] |
rs13206903 | 0.84[ASN][1000 genomes] |
rs13211770 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs13212301 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1358850 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs17079150 | 0.92[ASN][1000 genomes] |
rs17079156 | 0.88[AFR][1000 genomes] |
rs17079163 | 0.83[AFR][1000 genomes] |
rs17079166 | 0.83[AFR][1000 genomes] |
rs17079171 | 0.83[AFR][1000 genomes] |
rs17079173 | 0.83[AFR][1000 genomes] |
rs17079179 | 0.80[AFR][1000 genomes] |
rs17079180 | 0.80[AFR][1000 genomes] |
rs17079182 | 0.80[AFR][1000 genomes] |
rs17079183 | 0.80[AFR][1000 genomes] |
rs17090953 | 0.92[ASN][1000 genomes] |
rs1853149 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34059111 | 0.92[ASN][1000 genomes] |
rs34721599 | 0.83[AFR][1000 genomes] |
rs34900812 | 0.92[ASN][1000 genomes] |
rs34959842 | 0.92[ASN][1000 genomes] |
rs35476086 | 0.92[ASN][1000 genomes] |
rs35562167 | 0.92[ASN][1000 genomes] |
rs35874725 | 0.92[ASN][1000 genomes] |
rs35921544 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36111427 | 0.92[ASN][1000 genomes] |
rs36122926 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4640916 | 0.88[AFR][1000 genomes] |
rs67157504 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6913494 | 0.87[AFR][1000 genomes] |
rs6926675 | 0.84[AFR][1000 genomes] |
rs71554882 | 0.92[ASN][1000 genomes] |
rs71570850 | 0.92[ASN][1000 genomes] |
rs71570852 | 0.92[ASN][1000 genomes] |
rs71570854 | 0.84[ASN][1000 genomes] |
rs72951617 | 0.82[AFR][1000 genomes] |
rs72951630 | 0.83[AFR][1000 genomes] |
rs72951644 | 0.83[AFR][1000 genomes] |
rs72951645 | 0.82[AFR][1000 genomes] |
rs72955785 | 0.80[AFR][1000 genomes] |
rs72955789 | 0.80[AFR][1000 genomes] |
rs72955795 | 0.80[AFR][1000 genomes] |
rs72955798 | 0.80[AFR][1000 genomes] |
rs72955799 | 0.80[AFR][1000 genomes] |
rs72955802 | 0.80[AFR][1000 genomes] |
rs72957508 | 0.80[AFR][1000 genomes] |
rs72957515 | 0.80[AFR][1000 genomes] |
rs72957517 | 0.80[AFR][1000 genomes] |
rs72957518 | 0.80[AFR][1000 genomes] |
rs72957520 | 0.80[AFR][1000 genomes] |
rs72969416 | 0.88[AFR][1000 genomes] |
rs72969418 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969421 | 0.88[AFR][1000 genomes] |
rs72969428 | 0.88[AFR][1000 genomes] |
rs72969431 | 0.88[AFR][1000 genomes] |
rs72969434 | 0.88[AFR][1000 genomes] |
rs72969437 | 0.88[AFR][1000 genomes] |
rs72969454 | 0.88[AFR][1000 genomes] |
rs72969456 | 0.85[AFR][1000 genomes] |
rs9320600 | 0.88[AFR][1000 genomes] |
rs9320601 | 0.88[AFR][1000 genomes] |
rs9481706 | 0.88[AFR][1000 genomes] |
rs9481709 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9481711 | 0.80[AFR][1000 genomes] |
rs9481712 | 0.83[AFR][1000 genomes] |
rs9481713 | 0.83[AFR][1000 genomes] |
rs9489154 | 0.88[AFR][1000 genomes] |
rs9489156 | 0.88[AFR][1000 genomes] |
rs9489161 | 0.88[AFR][1000 genomes] |
rs9489162 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9489163 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9489165 | 0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9489167 | 0.84[AFR][1000 genomes] |
rs9489168 | 0.83[AFR][1000 genomes] |
rs9489169 | 0.83[AFR][1000 genomes] |
rs9489170 | 0.83[AFR][1000 genomes] |
rs9489172 | 0.83[AFR][1000 genomes] |
rs9489174 | 0.83[AFR][1000 genomes] |
rs9489175 | 0.83[AFR][1000 genomes] |
rs9489176 | 0.83[AFR][1000 genomes] |
rs9489177 | 0.83[AFR][1000 genomes] |
rs9489178 | 0.80[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532050 | chr6:117528154-118203005 | ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
2 | esv2763593 | chr6:117727550-117741495 | Weak transcription Strong transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv1032651 | chr6:117727550-117741495 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv1025551 | chr6:117730592-117741495 | Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:117723200-117737600 | Weak transcription | Lung | lung |
2 | chr6:117732400-117737200 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
3 | chr6:117735200-117736600 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr6:117735600-117736600 | Enhancers | HSMM | muscle |
5 | chr6:117735800-117736200 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
6 | chr6:117735800-117736400 | Enhancers | HepG2 | liver |
7 | chr6:117735800-117736600 | Enhancers | HMEC | breast |
8 | chr6:117735800-117736800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr6:117735800-117736800 | Enhancers | HSMMtube | muscle |