Variant report

Variant	rs4500902
Chromosome Location	chr2:186723376-186723377
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs1016410	0.90[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10165206	0.84[EUR][1000 genomes]
rs10173630	0.93[EUR][1000 genomes]
rs10173807	0.84[CEU][hapmap]
rs10192246	0.89[EUR][1000 genomes]
rs11893024	0.84[CEU][hapmap]
rs12328805	0.87[EUR][1000 genomes]
rs12464270	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12464403	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12464436	0.85[ASN][1000 genomes]
rs12464794	0.81[EUR][1000 genomes]
rs12464986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12466093	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs12474127	0.87[EUR][1000 genomes]
rs12475622	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12475648	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12478116	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12615971	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12988992	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12991700	0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12994796	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12998112	0.84[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs13002387	0.90[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs13003744	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs13004035	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13015006	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13026009	0.93[EUR][1000 genomes]
rs13027342	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs13031291	0.86[EUR][1000 genomes]
rs13387605	0.93[EUR][1000 genomes]
rs13411247	0.93[EUR][1000 genomes]
rs13429564	0.93[EUR][1000 genomes]
rs13432112	0.84[EUR][1000 genomes]
rs1861896	0.84[ASN][1000 genomes]
rs2216496	0.87[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs2255620	0.81[ASN][1000 genomes]
rs2287608	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2370475	0.82[ASN][1000 genomes]
rs2370505	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35986831	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36011205	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4233786	0.87[EUR][1000 genomes]
rs4263075	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4311032	0.93[EUR][1000 genomes]
rs4343435	0.87[EUR][1000 genomes]
rs4343438	1.00[CEU][hapmap];0.87[CHB][hapmap];0.93[EUR][1000 genomes]
rs4430905	0.87[EUR][1000 genomes]
rs4476313	0.87[EUR][1000 genomes]
rs4500903	0.87[EUR][1000 genomes]
rs4510179	0.93[EUR][1000 genomes]
rs4536613	0.93[EUR][1000 genomes]
rs4561628	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4571026	0.85[EUR][1000 genomes]
rs4577247	0.83[EUR][1000 genomes]
rs4619567	0.93[EUR][1000 genomes]
rs4627526	0.87[EUR][1000 genomes]
rs4666691	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4666692	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4666694	0.80[ASN][1000 genomes]
rs4666695	0.82[ASN][1000 genomes]
rs4666697	0.88[CEU][hapmap];0.81[CHB][hapmap];0.80[JPT][hapmap]
rs4667052	0.87[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4667056	0.93[EUR][1000 genomes]
rs4667057	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4667064	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4667065	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4667066	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4667067	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58696152	0.90[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs59190502	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs62199142	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs62199145	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs62200894	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62200949	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67196811	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6733946	0.80[ASN][1000 genomes]
rs6735082	0.80[ASN][1000 genomes]
rs6745546	0.81[CEU][hapmap];0.81[YRI][hapmap]
rs71407825	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7564229	0.92[EUR][1000 genomes]
rs7602728	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7605929	0.81[CEU][hapmap];0.81[YRI][hapmap]

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	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

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	chr2:186721800-186728200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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