Variant report

Variant	rs9936182
Chromosome Location	chr16:77269016-77269017
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1019565	0.90[ASN][1000 genomes]
rs11149971	0.90[ASN][1000 genomes]
rs11544783	0.90[ASN][1000 genomes]
rs11860898	0.82[ASN][1000 genomes]
rs11863718	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12931673	1.00[ASN][1000 genomes]
rs13329731	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13329816	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13330279	0.90[ASN][1000 genomes]
rs13330367	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13332812	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13336198	1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13337994	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13339324	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1428838	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1428839	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2017197	0.90[ASN][1000 genomes]
rs28539358	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61746433	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6564417	1.00[ASN][1000 genomes]
rs7184776	0.82[ASN][1000 genomes]
rs7188241	1.00[ASN][1000 genomes]
rs719053	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7198006	1.00[ASN][1000 genomes]
rs7198588	1.00[ASN][1000 genomes]
rs7201284	0.82[ASN][1000 genomes]
rs7203467	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73627401	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633620	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633624	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633633	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633644	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633647	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633654	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73633661	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7501191	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8048478	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9924958	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9929722	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9931082	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9931400	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9935921	1.00[ASN][1000 genomes]
rs9937408	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9937693	1.00[ASN][1000 genomes]
rs9938871	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065343	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv542965	chr16:76927295-77279747	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1055234	chr16:77003426-77467286	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
4	nsv1065048	chr16:77003426-77675163	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	esv2830376	chr16:77014551-77658185	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv1065149	chr16:77032082-77671890	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	nsv1062349	chr16:77039764-77458731	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv542967	chr16:77039764-77458731	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	nsv1056676	chr16:77139682-77854848	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
10	nsv1066258	chr16:77229953-77521919	Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv542968	chr16:77229953-77521919	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv524636	chr16:77258592-77297193	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS	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	chr16:77259200-77269800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:77261400-77270200	Weak transcription	A549	lung
3	chr16:77262400-77271200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:77268000-77269200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr16:77268200-77269200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr16:77268200-77269800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr16:77268200-77270200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr16:77268400-77269200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr16:77268400-77269200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr16:77268800-77269800	Weak transcription	HUVEC	blood vessel
11	chr16:77268800-77270000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr16:77269000-77269200	Enhancers	HUES6 Cell Line	embryonic stem cell

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