Variant report
Variant | rs12664078 |
---|---|
Chromosome Location | chr6:142817389-142817390 |
allele | C/T |
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 | chr6:142815726..142818546-chr6:142820153..142822884,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1013902 | 0.88[CEU][hapmap] |
rs1467720 | 0.98[EUR][1000 genomes] |
rs17071798 | 0.92[GIH][hapmap];0.82[TSI][hapmap] |
rs2294765 | 0.88[CEU][hapmap];0.92[GIH][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap] |
rs2294768 | 0.88[CEU][hapmap];0.92[GIH][hapmap];0.82[TSI][hapmap] |
rs2294770 | 0.92[GIH][hapmap];0.86[TSI][hapmap] |
rs2294773 | 0.92[GIH][hapmap];0.82[TSI][hapmap] |
rs2328339 | 0.98[EUR][1000 genomes] |
rs34701089 | 0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs4140531 | 0.88[CEU][hapmap] |
rs6913116 | 0.88[CEU][hapmap] |
rs714476 | 0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7758750 | 0.88[CEU][hapmap] |
rs9321871 | 0.81[EUR][1000 genomes] |
rs9373343 | 0.88[CEU][hapmap] |
rs9376689 | 0.88[CEU][hapmap] |
rs9385994 | 0.90[GIH][hapmap];0.82[TSI][hapmap] |
rs9389990 | 0.88[CEU][hapmap] |
rs9403384 | 0.92[GIH][hapmap];0.82[TSI][hapmap] |
rs9484645 | 0.81[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949088 | chr6:142561402-143128849 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1023426 | chr6:142813845-142940262 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:142817200-142817800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |