Variant report

Variant	rs6110985
Chromosome Location	chr20:16234466-16234467
allele	A/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:14)

rs_ID	r²[population]
rs16997379	0.85[ASN][1000 genomes]
rs6034427	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6043830	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6075037	0.91[ASN][1000 genomes]
rs6080190	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6105553	0.86[ASN][1000 genomes]
rs6110972	0.85[EUR][1000 genomes]
rs6110979	0.85[ASN][1000 genomes]
rs6110981	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6110983	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6135707	0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs6135712	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6135713	0.89[ASN][1000 genomes]
rs9973984	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833930	chr20:16134347-16302763	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:16234200-16235000	Enhancers	Fetal Heart	heart

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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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