Variant report

Variant	rs182610
Chromosome Location	chr14:80097636-80097637
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs17109649	0.96[ASN][1000 genomes]
rs172711	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1816146	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs184347	0.87[EUR][1000 genomes]
rs191991	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221436	0.88[EUR][1000 genomes]
rs221437	0.85[EUR][1000 genomes]
rs221439	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221440	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221442	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs221443	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs221444	0.88[EUR][1000 genomes]
rs221445	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs221446	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs221447	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221448	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs221449	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs221450	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221451	0.90[ASN][1000 genomes]
rs221452	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs221453	0.91[ASN][1000 genomes]
rs221455	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs221456	0.89[EUR][1000 genomes]
rs221457	0.93[ASN][1000 genomes]
rs221459	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs221465	0.86[ASN][1000 genomes]
rs221467	0.88[ASN][1000 genomes]
rs221468	0.87[ASN][1000 genomes]
rs221469	0.82[ASN][1000 genomes]
rs221471	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs221473	0.96[ASN][1000 genomes]
rs221474	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs221480	0.99[ASN][1000 genomes]
rs221481	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs221482	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs221483	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221484	0.93[EUR][1000 genomes]
rs221485	0.97[ASN][1000 genomes]
rs221497	0.96[ASN][1000 genomes]
rs221511	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs221512	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs221513	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs221514	0.90[EUR][1000 genomes]
rs221516	0.87[ASN][1000 genomes]
rs2543584	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55933035	0.89[ASN][1000 genomes]
rs69029	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs918937	0.89[EUR][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	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv869542	chr14:80009619-80118315	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:80095000-80098600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:80096000-80097800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr14:80096600-80099600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr14:80097200-80098000	Enhancers	Placenta	Placenta
5	chr14:80097600-80098000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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