Variant report

Variant	rs1360814
Chromosome Location	chr13:80403917-80403918
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12430995	0.90[ASN][1000 genomes]
rs12876803	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1335282	0.95[CHB][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1360812	0.95[ASN][1000 genomes]
rs1889642	0.94[ASN][1000 genomes]
rs2329139	0.89[ASN][1000 genomes]
rs4619276	0.89[ASN][1000 genomes]
rs9530980	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9530981	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9545217	0.94[ASN][1000 genomes]
rs9545219	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9545224	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9545241	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9545244	0.95[CHB][hapmap];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9574501	0.84[EUR][1000 genomes];0.81[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	nsv900588	chr13:80216846-80421340	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv900590	chr13:80342186-80421340	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1043768	chr13:80398379-80447095	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr13:80403600-80408400	Weak transcription	H1 Derived Neuronal Progenitor 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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