Variant report

Variant	rs10134529
Chromosome Location	chr14:40408540-40408541
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10135401	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10139130	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10150979	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10151173	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10220364	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1157666	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1157667	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11850290	1.00[ASN][1000 genomes]
rs11851283	1.00[ASN][1000 genomes]
rs17092098	1.00[ASN][1000 genomes]
rs17109971	1.00[ASN][1000 genomes]
rs17109976	1.00[ASN][1000 genomes]
rs17109992	1.00[ASN][1000 genomes]
rs1951324	1.00[ASN][1000 genomes]
rs1951334	1.00[ASN][1000 genomes]
rs1957223	1.00[ASN][1000 genomes]
rs1957227	1.00[ASN][1000 genomes]
rs1998254	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2415569	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28813996	1.00[ASN][1000 genomes]
rs2899897	1.00[ASN][1000 genomes]
rs4134257	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4548776	1.00[ASN][1000 genomes]
rs55660421	1.00[ASN][1000 genomes]
rs55929735	1.00[ASN][1000 genomes]
rs56380567	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57214743	1.00[ASN][1000 genomes]
rs58733214	1.00[ASN][1000 genomes]
rs61144770	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7144491	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530658	chr14:40214958-40734070	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2751272	chr14:40216880-40913230	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv901660	chr14:40302876-40410765	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1047949	chr14:40307360-40474579	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1050737	chr14:40360366-40428708	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	nsv1048773	chr14:40360366-40433422	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv1035957	chr14:40362391-40433422	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:40408200-40409000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr14:40408400-40408800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:40408400-40409000	Enhancers	Aorta	Aorta

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