Variant report

Variant	rs13336602
Chromosome Location	chr16:79861682-79861683
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:79857005..79859687-chr16:79861505..79863503,2	K562	blood:

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10871380	0.84[AFR][1000 genomes]
rs11150199	0.90[AFR][1000 genomes]
rs11150200	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs11150201	0.87[AFR][1000 genomes]
rs11150202	0.87[AFR][1000 genomes]
rs11150203	0.87[AFR][1000 genomes]
rs11150204	0.87[AFR][1000 genomes]
rs11150205	0.87[AFR][1000 genomes]
rs11150206	0.87[AFR][1000 genomes]
rs11150207	0.87[AFR][1000 genomes]
rs11150208	0.82[AFR][1000 genomes]
rs11150209	0.82[AFR][1000 genomes]
rs11150210	0.81[AFR][1000 genomes]
rs11150211	0.87[AFR][1000 genomes]
rs11150212	0.87[AFR][1000 genomes]
rs11150213	0.87[AFR][1000 genomes]
rs11150214	0.87[AFR][1000 genomes]
rs11150215	0.80[AFR][1000 genomes]
rs11150216	0.87[AFR][1000 genomes]
rs11150219	0.97[AFR][1000 genomes]
rs11150220	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs1134715	0.87[AFR][1000 genomes]
rs11642817	0.97[AFR][1000 genomes]
rs11643810	0.90[AFR][1000 genomes]
rs11648556	0.84[AFR][1000 genomes]
rs11648855	0.87[AFR][1000 genomes]
rs11860693	0.90[AFR][1000 genomes]
rs11862561	0.84[AFR][1000 genomes]
rs11862593	0.90[AFR][1000 genomes]
rs11863874	0.87[AFR][1000 genomes]
rs11866244	0.97[AFR][1000 genomes]
rs12444097	0.90[AFR][1000 genomes]
rs12444100	0.90[AFR][1000 genomes]
rs12444123	0.82[AFR][1000 genomes]
rs12446125	0.90[AFR][1000 genomes]
rs12595956	0.87[AFR][1000 genomes]
rs12597506	0.87[AFR][1000 genomes]
rs12598926	0.87[AFR][1000 genomes]
rs12919529	0.84[AFR][1000 genomes]
rs12920397	0.90[AFR][1000 genomes]
rs12923698	0.84[AFR][1000 genomes]
rs12925344	0.84[AFR][1000 genomes]
rs12928764	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12930441	0.91[AFR][1000 genomes]
rs12931444	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12931584	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12934885	0.90[AFR][1000 genomes]
rs3935177	0.90[AFR][1000 genomes]
rs4243184	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4299168	0.87[AFR][1000 genomes]
rs4392086	0.87[AFR][1000 genomes]
rs4538028	0.87[AFR][1000 genomes]
rs4584830	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs4611477	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4636922	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4888047	0.90[AFR][1000 genomes]
rs4888048	0.87[AFR][1000 genomes]
rs4888049	0.87[AFR][1000 genomes]
rs4889029	0.90[AFR][1000 genomes]
rs4889030	0.90[AFR][1000 genomes]
rs4889031	0.90[AFR][1000 genomes]
rs4889032	0.87[AFR][1000 genomes]
rs4889033	0.87[AFR][1000 genomes]
rs4889034	0.87[AFR][1000 genomes]
rs4889035	0.87[AFR][1000 genomes]
rs6564706	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7187906	0.87[AFR][1000 genomes]
rs7191989	0.87[AFR][1000 genomes]
rs8043824	0.97[AFR][1000 genomes]
rs8059641	0.81[AMR][1000 genomes]
rs8063960	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9939031	0.97[AFR][1000 genomes];0.82[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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv530714	chr16:79661581-79925435	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv833296	chr16:79692236-79889727	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv833297	chr16:79732501-79920419	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1059511	chr16:79847882-79925436	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv542984	chr16:79847882-79925436	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv573290	chr16:79853267-79939504	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79860200-79862000	Enhancers	Fetal Lung	lung
2	chr16:79860800-79861800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr16:79861400-79861800	Enhancers	NHDF-Ad	bronchial

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