Variant report

Variant	rs59190502
Chromosome Location	chr2:186761497-186761498
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	chr2:186760390..186763157-chr2:186764375..186766387,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1016410	0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs12464270	0.90[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs12464403	0.86[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12464436	0.84[ASN][1000 genomes]
rs12464986	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12466093	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12475622	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12475648	0.86[ASN][1000 genomes]
rs12478116	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12988992	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12991700	0.80[ASN][1000 genomes]
rs12994796	0.94[ASN][1000 genomes]
rs12998112	0.82[ASN][1000 genomes]
rs13002387	0.83[ASN][1000 genomes]
rs13003744	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs13004035	0.94[ASN][1000 genomes]
rs13015006	0.93[ASN][1000 genomes]
rs13027342	0.82[ASN][1000 genomes]
rs1861896	0.82[ASN][1000 genomes]
rs2287608	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2370505	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs35986831	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs36011205	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4263075	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4500902	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4561628	0.97[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4666691	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4666692	0.96[ASN][1000 genomes]
rs4666694	0.82[ASN][1000 genomes]
rs4666695	0.83[ASN][1000 genomes]
rs4667057	0.97[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4667064	0.94[ASN][1000 genomes]
rs4667065	0.94[ASN][1000 genomes]
rs4667066	0.94[ASN][1000 genomes]
rs4667067	0.86[ASN][1000 genomes]
rs58696152	0.83[ASN][1000 genomes]
rs62199142	0.83[ASN][1000 genomes]
rs62199145	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs62200894	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs62200949	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs67196811	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs71407825	0.83[ASN][1000 genomes]
rs7602728	0.83[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	nsv1007052	chr2:186441382-186864390	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv584019	chr2:186445393-186866874	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1009118	chr2:186450293-186864390	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1008230	chr2:186474069-186818718	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv536076	chr2:186474069-186818718	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv584021	chr2:186475590-186866841	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv875545	chr2:186566024-187280164	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	esv1797599	chr2:186618494-186882821	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv817325	chr2:186625679-187200841	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv868949	chr2:186657142-187327560	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv1002243	chr2:186692815-187150225	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
12	nsv536077	chr2:186692815-187150225	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv998624	chr2:186735464-186845432	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv932296	chr2:186737443-187265790	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv584023	chr2:186750735-186851224	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv875546	chr2:186756348-186892254	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186716800-186767200	Weak transcription	Ovary	ovary
2	chr2:186760800-186761600	Enhancers	HepG2	liver

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