Variant report

Variant	rs35559119
Chromosome Location	chr2:133923590-133923591
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10803536	0.91[ASN][1000 genomes]
rs10928441	0.91[ASN][1000 genomes]
rs10928442	0.94[ASN][1000 genomes]
rs12052593	0.82[ASN][1000 genomes]
rs12053035	0.93[ASN][1000 genomes]
rs12611686	0.95[ASN][1000 genomes]
rs12613747	0.88[ASN][1000 genomes]
rs12621765	0.81[ASN][1000 genomes]
rs12622633	0.88[ASN][1000 genomes]
rs12622679	0.90[ASN][1000 genomes]
rs12624035	0.81[ASN][1000 genomes]
rs12991216	0.90[ASN][1000 genomes]
rs12996075	0.86[ASN][1000 genomes]
rs13001406	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13004057	0.90[ASN][1000 genomes]
rs13021439	0.81[ASN][1000 genomes]
rs13031924	0.91[ASN][1000 genomes]
rs1434225	0.86[ASN][1000 genomes]
rs1434228	0.91[ASN][1000 genomes]
rs16857026	0.82[ASN][1000 genomes]
rs16857027	0.82[ASN][1000 genomes]
rs16857341	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16857667	0.93[ASN][1000 genomes]
rs16857684	0.90[ASN][1000 genomes]
rs16857813	0.95[ASN][1000 genomes]
rs16857829	0.95[ASN][1000 genomes]
rs16857909	0.95[ASN][1000 genomes]
rs16857911	0.95[ASN][1000 genomes]
rs1975218	0.89[ASN][1000 genomes]
rs1975219	0.82[ASN][1000 genomes]
rs1975220	0.82[ASN][1000 genomes]
rs1975221	0.82[ASN][1000 genomes]
rs2117307	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2117308	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2217748	0.82[ASN][1000 genomes]
rs2278454	0.81[ASN][1000 genomes]
rs2278455	0.82[ASN][1000 genomes]
rs2278456	0.82[ASN][1000 genomes]
rs34497516	0.86[ASN][1000 genomes]
rs34962273	0.84[ASN][1000 genomes]
rs35101763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35385294	0.86[ASN][1000 genomes]
rs35635401	0.93[ASN][1000 genomes]
rs35976316	0.92[ASN][1000 genomes]
rs35986779	0.81[ASN][1000 genomes]
rs4283469	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4953871	0.80[ASN][1000 genomes]
rs4953874	0.81[ASN][1000 genomes]
rs4953876	0.92[ASN][1000 genomes]
rs4954027	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4954028	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4954030	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4954033	0.93[ASN][1000 genomes]
rs6430394	0.86[ASN][1000 genomes]
rs6430397	0.91[ASN][1000 genomes]
rs6430398	0.95[ASN][1000 genomes]
rs6715483	0.93[ASN][1000 genomes]
rs6733792	0.95[ASN][1000 genomes]
rs6735052	0.95[ASN][1000 genomes]
rs6744186	0.93[ASN][1000 genomes]
rs6744536	0.93[ASN][1000 genomes]
rs6749758	0.94[ASN][1000 genomes]
rs6753721	0.92[ASN][1000 genomes]
rs71413533	0.81[ASN][1000 genomes]
rs71413534	0.88[ASN][1000 genomes]
rs71413537	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71413541	0.90[ASN][1000 genomes]
rs71413543	0.95[ASN][1000 genomes]
rs71413544	0.91[ASN][1000 genomes]
rs7568295	0.80[ASN][1000 genomes]
rs7585526	0.82[ASN][1000 genomes]
rs7592507	0.88[ASN][1000 genomes]
rs7597720	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916805	chr2:133664765-133924973	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875139	chr2:133777866-133929225	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv949546	chr2:133798832-133933491	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1008004	chr2:133827250-133954810	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv949629	chr2:133830379-134014961	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1001601	chr2:133838626-134005959	Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv948851	chr2:133864452-133955999	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv583167	chr2:133864452-133957689	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv997821	chr2:133868822-134360220	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
10	nsv535927	chr2:133868822-134360220	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
11	nsv1002488	chr2:133890159-134275312	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv535928	chr2:133890159-134275312	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv1011100	chr2:133900062-134046163	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
14	nsv459463	chr2:133905985-133933462	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv583168	chr2:133905985-133933462	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	esv3375790	chr2:133906915-134222833	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr2:133921600-133923600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:133922600-133924800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:133923000-133924600	Enhancers	Osteobl	bone
4	chr2:133923000-133924800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:133923400-133923800	Enhancers	NHDF-Ad	bronchial

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