Variant report

Variant	rs770931
Chromosome Location	chr6:16856141-16856142
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10949386	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12204538	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1240835	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1240839	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12526123	0.88[ASN][1000 genomes]
rs2797805	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57192327	0.88[ASN][1000 genomes]
rs6459487	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs770935	0.93[ASN][1000 genomes]
rs770937	0.93[ASN][1000 genomes]
rs770938	0.91[ASN][1000 genomes]
rs9464950	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9464951	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9464952	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9477235	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:16852400-16856400	Weak transcription	Adipose Nuclei	Adipose
2	chr6:16855200-16856200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:16855200-16857200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:16856000-16856400	Enhancers	GM12878-XiMat	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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