Variant report
Variant | rs1233668 |
---|---|
Chromosome Location | chr6:28144642-28144643 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000176933 | Chromatin interaction |
ENSG00000238610 | Chromatin interaction |
ENSG00000226314 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1144707 | 1.00[AMR][1000 genomes] |
rs1150667 | 1.00[AMR][1000 genomes] |
rs1150675 | 1.00[AMR][1000 genomes] |
rs1150677 | 1.00[AMR][1000 genomes] |
rs1150681 | 1.00[AMR][1000 genomes] |
rs1150706 | 1.00[AMR][1000 genomes] |
rs12208060 | 1.00[AMR][1000 genomes] |
rs1225589 | 1.00[AMR][1000 genomes] |
rs1225601 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1233663 | 1.00[AMR][1000 genomes] |
rs1778485 | 1.00[AMR][1000 genomes] |
rs213229 | 1.00[AMR][1000 genomes] |
rs213234 | 1.00[AMR][1000 genomes] |
rs213242 | 1.00[AMR][1000 genomes] |
rs2394048 | 1.00[AMR][1000 genomes] |
rs2531829 | 1.00[AMR][1000 genomes] |
rs2799080 | 1.00[AMR][1000 genomes] |
rs2859361 | 1.00[AMR][1000 genomes] |
rs4713154 | 1.00[AMR][1000 genomes] |
rs59183152 | 1.00[AMR][1000 genomes] |
rs6902266 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7740205 | 0.91[AFR][1000 genomes] |
rs7747984 | 0.91[AFR][1000 genomes] |
rs7760347 | 0.91[AFR][1000 genomes] |
rs7769304 | 0.91[AFR][1000 genomes] |
rs853675 | 1.00[AMR][1000 genomes] |
rs853677 | 1.00[AMR][1000 genomes] |
rs853680 | 1.00[AMR][1000 genomes] |
rs853686 | 1.00[AMR][1000 genomes] |
rs853691 | 1.00[AMR][1000 genomes] |
rs853692 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3384757 | chr6:28143357-28145067 | Weak transcription | TF binding regionChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:28129800-28145400 | Weak transcription | Brain Angular Gyrus | brain |
2 | chr6:28138000-28145600 | Weak transcription | K562 | blood |
3 | chr6:28139400-28145600 | Weak transcription | Brain Inferior Temporal Lobe | brain |