Variant report
Variant | rs6997547 |
---|---|
Chromosome Location | chr8:64314162-64314163 |
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 | chr8:64312553..64315389-chr8:64317911..64320594,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10093298 | 0.94[EUR][1000 genomes] |
rs10095044 | 0.93[EUR][1000 genomes] |
rs10103710 | 0.87[EUR][1000 genomes] |
rs10112423 | 0.96[EUR][1000 genomes] |
rs1013259 | 0.93[EUR][1000 genomes] |
rs10156375 | 0.85[EUR][1000 genomes] |
rs1030584 | 0.86[EUR][1000 genomes] |
rs1030585 | 0.86[EUR][1000 genomes] |
rs1030586 | 0.86[EUR][1000 genomes] |
rs1030587 | 0.83[ASN][1000 genomes] |
rs10441558 | 0.97[EUR][1000 genomes] |
rs10808732 | 0.92[EUR][1000 genomes] |
rs10957282 | 0.87[EUR][1000 genomes] |
rs10957283 | 0.87[EUR][1000 genomes] |
rs10957285 | 0.93[EUR][1000 genomes] |
rs11775060 | 0.87[CEU][hapmap];0.92[EUR][1000 genomes] |
rs11777208 | 0.84[EUR][1000 genomes] |
rs11777936 | 0.87[CEU][hapmap];0.92[EUR][1000 genomes] |
rs11779425 | 1.00[CEU][hapmap];0.97[EUR][1000 genomes] |
rs11782289 | 0.93[EUR][1000 genomes] |
rs11783042 | 1.00[CEU][hapmap];0.97[EUR][1000 genomes] |
rs11783055 | 1.00[CEU][hapmap];0.97[EUR][1000 genomes] |
rs11786252 | 1.00[CEU][hapmap];0.97[EUR][1000 genomes] |
rs12544518 | 0.90[EUR][1000 genomes] |
rs12545091 | 0.96[CEU][hapmap];0.97[EUR][1000 genomes] |
rs12549069 | 0.93[EUR][1000 genomes] |
rs12550189 | 0.98[EUR][1000 genomes] |
rs13250116 | 0.93[EUR][1000 genomes] |
rs13265562 | 0.96[CEU][hapmap];0.93[EUR][1000 genomes] |
rs13267865 | 0.93[EUR][1000 genomes] |
rs13277482 | 0.87[EUR][1000 genomes] |
rs1431591 | 0.92[EUR][1000 genomes] |
rs16930415 | 0.86[EUR][1000 genomes] |
rs2354894 | 0.88[CEU][hapmap];0.92[EUR][1000 genomes] |
rs28540225 | 0.86[EUR][1000 genomes] |
rs28877014 | 0.93[EUR][1000 genomes] |
rs35674021 | 0.87[EUR][1000 genomes] |
rs4737646 | 0.93[EUR][1000 genomes] |
rs4739089 | 0.96[CEU][hapmap];0.95[EUR][1000 genomes] |
rs4739090 | 0.95[EUR][1000 genomes] |
rs4739091 | 0.87[CEU][hapmap];0.92[EUR][1000 genomes] |
rs56033239 | 0.84[EUR][1000 genomes] |
rs6472093 | 0.83[EUR][1000 genomes] |
rs6472094 | 0.83[EUR][1000 genomes] |
rs6472095 | 0.82[EUR][1000 genomes] |
rs6472096 | 0.83[EUR][1000 genomes] |
rs6472097 | 0.83[EUR][1000 genomes] |
rs6472103 | 0.90[EUR][1000 genomes] |
rs6472104 | 0.89[EUR][1000 genomes] |
rs6981013 | 0.86[EUR][1000 genomes] |
rs6981563 | 0.85[EUR][1000 genomes] |
rs6987680 | 0.93[EUR][1000 genomes] |
rs6993493 | 0.84[EUR][1000 genomes] |
rs6994236 | 0.92[CEU][hapmap];0.93[EUR][1000 genomes] |
rs7006972 | 0.95[EUR][1000 genomes] |
rs7016013 | 0.84[EUR][1000 genomes] |
rs7459926 | 0.84[EUR][1000 genomes] |
rs7460026 | 0.83[EUR][1000 genomes] |
rs7462242 | 0.92[EUR][1000 genomes] |
rs7464324 | 0.84[EUR][1000 genomes] |
rs7818456 | 0.83[EUR][1000 genomes] |
rs7825481 | 0.92[EUR][1000 genomes] |
rs7834350 | 0.88[CEU][hapmap];0.92[EUR][1000 genomes] |
rs7840470 | 0.90[EUR][1000 genomes] |
rs7841852 | 1.00[CEU][hapmap];0.97[EUR][1000 genomes] |
rs7841909 | 0.83[EUR][1000 genomes] |
rs891691 | 0.94[EUR][1000 genomes] |
rs9298075 | 0.87[EUR][1000 genomes] |
rs9298077 | 0.96[CEU][hapmap];0.96[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv890967 | chr8:64107847-64454446 | Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv6229 | chr8:64282018-64326530 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:64310000-64314400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr8:64310200-64314200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
3 | chr8:64312600-64314200 | Weak transcription | GM12878-XiMat | blood |