Variant report

Variant	rs9864756
Chromosome Location	chr3:69179321-69179322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11706756	0.87[ASN][1000 genomes]
rs17005397	0.97[ASN][1000 genomes]
rs34550101	0.97[ASN][1000 genomes]
rs4525874	0.98[ASN][1000 genomes]
rs4855355	0.97[ASN][1000 genomes]
rs4855357	0.84[ASN][1000 genomes]
rs4855548	0.97[ASN][1000 genomes]
rs4855549	0.94[ASN][1000 genomes]
rs4855550	0.95[ASN][1000 genomes]
rs5017791	0.90[ASN][1000 genomes]
rs5017792	0.90[ASN][1000 genomes]
rs55978846	0.97[ASN][1000 genomes]
rs58798960	0.97[ASN][1000 genomes]
rs60204248	0.97[ASN][1000 genomes]
rs61207882	0.97[ASN][1000 genomes]
rs6762052	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6767493	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6778830	0.96[ASN][1000 genomes]
rs6779171	0.97[ASN][1000 genomes]
rs6806271	0.82[ASN][1000 genomes]
rs6808756	0.82[ASN][1000 genomes]
rs7613159	0.95[ASN][1000 genomes]
rs7638997	0.86[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs881804	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs937863	0.97[ASN][1000 genomes]
rs9815992	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9825485	0.98[ASN][1000 genomes]
rs9843043	0.98[ASN][1000 genomes]
rs9853232	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876933	chr3:69059023-69227379	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv521439	chr3:69171803-69185740	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69178000-69193600	Weak transcription	Psoas Muscle	Psoas
2	chr3:69178400-69180000	Weak transcription	Placenta	Placenta
3	chr3:69179200-69180000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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Input of quick search could be:

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

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