Variant report

Variant	rs4933549
Chromosome Location	chr10:91849118-91849119
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10509590	0.85[ASN][1000 genomes]
rs10509594	0.85[ASN][1000 genomes]
rs10748536	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10881747	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10881752	0.85[ASN][1000 genomes]
rs11185971	0.85[ASN][1000 genomes]
rs11185976	0.85[ASN][1000 genomes]
rs11185994	0.85[ASN][1000 genomes]
rs11186005	0.85[ASN][1000 genomes]
rs11186008	0.85[ASN][1000 genomes]
rs11186014	0.85[ASN][1000 genomes]
rs11186017	0.85[ASN][1000 genomes]
rs11186018	0.85[ASN][1000 genomes]
rs11186019	0.85[ASN][1000 genomes]
rs11498650	0.85[ASN][1000 genomes]
rs11593543	0.85[ASN][1000 genomes]
rs11597813	0.85[ASN][1000 genomes]
rs12244345	0.85[ASN][1000 genomes]
rs12245099	0.85[ASN][1000 genomes]
rs12246345	0.85[ASN][1000 genomes]
rs12246861	0.85[ASN][1000 genomes]
rs12247466	0.85[ASN][1000 genomes]
rs12253356	0.85[ASN][1000 genomes]
rs12256658	0.85[ASN][1000 genomes]
rs12259650	0.85[ASN][1000 genomes]
rs12265445	0.85[ASN][1000 genomes]
rs12267667	0.85[ASN][1000 genomes]
rs12718335	0.85[ASN][1000 genomes]
rs12761190	0.85[ASN][1000 genomes]
rs12762952	0.85[ASN][1000 genomes]
rs12765811	0.85[ASN][1000 genomes]
rs12777990	0.85[ASN][1000 genomes]
rs12784707	0.85[ASN][1000 genomes]
rs1329163	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17506260	0.85[ASN][1000 genomes]
rs1831246	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2419361	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2419367	0.92[EUR][1000 genomes]
rs28846383	0.85[ASN][1000 genomes]
rs34102587	0.85[ASN][1000 genomes]
rs34212831	0.85[ASN][1000 genomes]
rs34337661	0.85[ASN][1000 genomes]
rs35784625	0.85[ASN][1000 genomes]
rs4534486	0.85[ASN][1000 genomes]
rs4933174	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55940458	0.85[ASN][1000 genomes]
rs56070739	0.85[ASN][1000 genomes]
rs61870189	0.85[ASN][1000 genomes]
rs61870192	0.85[ASN][1000 genomes]
rs67388825	0.85[ASN][1000 genomes]
rs7070751	0.85[ASN][1000 genomes]
rs7079268	0.85[ASN][1000 genomes]
rs7080686	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7080966	0.85[ASN][1000 genomes]
rs7081619	0.85[ASN][1000 genomes]
rs7081751	0.85[ASN][1000 genomes]
rs7086058	0.85[ASN][1000 genomes]
rs7090923	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7101251	0.85[ASN][1000 genomes]
rs7894193	0.85[ASN][1000 genomes]
rs7894782	0.85[ASN][1000 genomes]
rs7900053	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7900680	0.85[ASN][1000 genomes]
rs7901005	0.85[ASN][1000 genomes]
rs7913850	0.85[ASN][1000 genomes]
rs9971285	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043571	chr10:91568555-92036154	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv551874	chr10:91570211-92036154	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv949678	chr10:91589048-92016474	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv895883	chr10:91610601-92195828	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1039731	chr10:91645718-92198264	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv540743	chr10:91645718-92198264	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv467430	chr10:91681344-92297943	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv551875	chr10:91681344-92297943	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	esv1839881	chr10:91762226-91861413	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv519094	chr10:91769945-91927196	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91820000-91860000	Weak transcription	Primary B cells from cord blood	blood
2	chr10:91846800-91849400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr10:91847200-91849600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:91847200-91852000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr10:91847200-91869400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr10:91847600-91851800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr10:91848000-91849200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:91848000-91849200	Weak transcription	HMEC	breast
9	chr10:91848000-91852200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:91848800-91849600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr10:91849000-91849200	Enhancers	NHLF	lung
12	chr10:91849000-91850400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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