Variant report

Variant	rs569016
Chromosome Location	chr13:70102087-70102088
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11617665	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2150149	0.87[ASN][1000 genomes]
rs2483326	0.98[ASN][1000 genomes]
rs352257	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs520469	0.93[ASN][1000 genomes]
rs66513806	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7321900	0.88[EUR][1000 genomes]
rs9529599	0.81[ASN][1000 genomes]
rs9541977	0.80[ASN][1000 genomes]
rs9564573	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9572176	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9572177	0.92[EUR][1000 genomes];0.82[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	nsv1045844	chr13:70038096-70405435	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv1833005	chr13:70090874-70180509	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	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	chr13:70101600-70102200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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