Variant report
Variant | rs10951164 |
---|---|
Chromosome Location | chr7:27443337-27443338 |
allele | C/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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | 7:27238414-27242313..7:27439194-27449722 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000106031 | Chromatin interaction |
ENSG00000243766 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10252971 | 0.94[EUR][1000 genomes] |
rs10268902 | 1.00[ASN][1000 genomes] |
rs10271302 | 0.81[JPT][hapmap] |
rs10280925 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes] |
rs1034660 | 0.89[ASN][1000 genomes] |
rs12700805 | 1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes] |
rs17439381 | 0.93[ASN][1000 genomes] |
rs1966331 | 0.83[ASN][1000 genomes] |
rs2074337 | 0.95[EUR][1000 genomes] |
rs2074338 | 0.95[EUR][1000 genomes] |
rs34226948 | 0.86[ASN][1000 genomes] |
rs3846999 | 0.86[ASN][1000 genomes] |
rs4719891 | 0.88[EUR][1000 genomes] |
rs6953463 | 0.93[EUR][1000 genomes] |
rs6957441 | 0.93[CEU][hapmap];0.94[EUR][1000 genomes] |
rs6957649 | 0.93[CEU][hapmap];0.94[EUR][1000 genomes] |
rs6963552 | 0.90[ASN][1000 genomes] |
rs757143 | 0.82[ASN][1000 genomes] |
rs7798437 | 0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531024 | chr7:27194426-27461954 | Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 148 gene(s) | inside rSNPs | diseases |
2 | nsv830930 | chr7:27395838-27587355 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
No data |