Variant report

Variant	rs4899455
Chromosome Location	chr14:40336070-40336071
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10140474	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10147318	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11625949	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11626528	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12885560	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1957200	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1957201	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1957202	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1957204	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2104106	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4899456	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4903075	0.85[AMR][1000 genomes]
rs4903101	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4903103	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6571968	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6571969	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6571970	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6571971	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6571972	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6571973	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7145741	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7158647	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8009983	0.85[AMR][1000 genomes]
rs8015888	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9323007	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs933038	0.85[AMR][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	nsv832776	chr14:40203172-40342229	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	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
3	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
4	nsv1040418	chr14:40293500-40339528	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv525070	chr14:40302876-40353756	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv901660	chr14:40302876-40410765	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1047949	chr14:40307360-40474579	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	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	chr14:40333400-40348600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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