Variant report

Variant	rs6792468
Chromosome Location	chr3:156776416-156776417
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10513500	1.00[ASN][1000 genomes]
rs10513501	1.00[ASN][1000 genomes]
rs10513502	1.00[ASN][1000 genomes]
rs1482850	1.00[ASN][1000 genomes]
rs1482862	1.00[ASN][1000 genomes]
rs16826968	1.00[ASN][1000 genomes]
rs57791022	1.00[ASN][1000 genomes]
rs59981665	1.00[ASN][1000 genomes]
rs73873771	1.00[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	esv3349885	chr3:156685409-156878910	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 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	chr3:156776000-156777000	Enhancers	GM12878-XiMat	blood
2	chr3:156776200-156776800	Enhancers	hESC Derived CD184+ Endoderm Cultured 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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