Variant report

Variant	rs12515167
Chromosome Location	chr5:113237400-113237401
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13165947	0.88[ASN][1000 genomes]
rs13166844	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13169639	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13172165	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13187257	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35198837	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35253026	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6882254	0.80[EUR][1000 genomes]
rs6887668	0.84[EUR][1000 genomes]
rs73249072	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73252641	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7723550	0.96[EUR][1000 genomes];0.88[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	nsv471042	chr5:113160490-113440892	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:113236800-113238600	Weak transcription	H1 BMP4 Derived Mesendoderm 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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