Variant report

Variant	rs4523064
Chromosome Location	chr6:165363350-165363351
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10946040	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10946041	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10946042	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10946051	0.83[ASN][1000 genomes]
rs12203926	0.83[ASN][1000 genomes]
rs2322644	0.83[ASN][1000 genomes]
rs56169436	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57819836	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9347050	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9347946	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9355521	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9356318	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9365824	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv605232	chr6:164994771-165401154	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv886925	chr6:165319631-165705488	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv886926	chr6:165358270-165478051	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165361000-165364600	Weak transcription	HSMMtube	muscle

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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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