Variant report

Variant	rs34459643
Chromosome Location	chr14:65579414-65579415
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:65567727..65571769-chr14:65574635..65579781,8	MCF-7	breast:
2	chr14:65574956..65578020-chr14:65578405..65580427,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000125952	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10143198	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10151162	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11158577	0.85[EUR][1000 genomes]
rs1124751	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1124752	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11623603	0.80[EUR][1000 genomes]
rs11626156	0.82[EUR][1000 genomes]
rs1256417	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1270074	0.80[EUR][1000 genomes]
rs1953232	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1957948	0.82[EUR][1000 genomes]
rs1957949	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1998688	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2151755	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2763888	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2781373	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2781374	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2781375	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2898863	0.81[EUR][1000 genomes]
rs35410051	0.83[EUR][1000 genomes]
rs35520739	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4902359	0.80[EUR][1000 genomes]
rs4902362	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4902363	0.80[EUR][1000 genomes]
rs7145112	0.82[EUR][1000 genomes]
rs7146939	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7150646	0.80[EUR][1000 genomes]
rs7152277	0.82[EUR][1000 genomes]
rs7158239	0.80[EUR][1000 genomes]
rs7159443	0.83[EUR][1000 genomes]
rs8004805	0.88[EUR][1000 genomes]
rs8005829	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8008095	0.81[EUR][1000 genomes]
rs8010213	0.83[EUR][1000 genomes]
rs8015921	0.81[EUR][1000 genomes]
rs868814	0.82[EUR][1000 genomes]
rs942626	0.83[EUR][1000 genomes]
rs942628	0.82[EUR][1000 genomes]
rs942629	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs998247	0.86[AMR][1000 genomes];0.89[EUR][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	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 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	chr14:65577600-65581000	Weak transcription	K562	blood

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