Variant report

Variant	rs61366297
Chromosome Location	chr3:155802867-155802868
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13062621	1.00[AMR][1000 genomes]
rs34921805	1.00[AMR][1000 genomes]
rs35639351	1.00[AMR][1000 genomes]
rs56811290	0.82[ASN][1000 genomes]
rs61623796	0.82[ASN][1000 genomes]
rs62284916	0.80[ASN][1000 genomes]
rs62284918	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62284919	0.82[ASN][1000 genomes]
rs62284920	0.82[ASN][1000 genomes]
rs62284931	1.00[EUR][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	nsv592084	chr3:155751484-155830578	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr3:155800200-155811800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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