Variant report

Variant	rs13254656
Chromosome Location	chr8:58604747-58604748
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11785847	0.83[ASN][1000 genomes]
rs12680410	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13248067	0.84[ASN][1000 genomes]
rs13252002	0.91[ASN][1000 genomes]
rs13256714	0.80[EUR][1000 genomes]
rs13258879	0.84[ASN][1000 genomes]
rs13263280	0.84[ASN][1000 genomes]
rs13266423	0.98[ASN][1000 genomes]
rs34163390	0.84[ASN][1000 genomes]
rs4131859	0.84[ASN][1000 genomes]
rs4266637	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4546648	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4629855	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4737466	0.82[ASN][1000 genomes]
rs4738611	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62514331	0.81[EUR][1000 genomes]
rs6471640	0.84[ASN][1000 genomes]
rs7005602	0.91[ASN][1000 genomes]
rs9650186	0.82[AMR][1000 genomes];0.84[EUR][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	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv890937	chr8:58600994-58695807	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58602000-58616200	Weak transcription	Aorta	Aorta
2	chr8:58603200-58606400	Weak transcription	Pancreas	Pancrea

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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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