Variant report

Variant	rs1880915
Chromosome Location	chr2:178813992-178813993
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10930814	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs11695211	0.86[CHD][hapmap];0.86[JPT][hapmap]
rs12463866	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs12469439	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs1369520	0.87[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs1405643	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs1405644	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs1405645	0.87[CHB][hapmap];0.86[CHD][hapmap];0.86[JPT][hapmap]
rs1405646	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs1435575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1438040	0.91[MEX][hapmap]
rs1534290	0.96[CEU][hapmap];0.84[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs16865995	0.96[CEU][hapmap];0.84[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs16866042	0.92[CEU][hapmap];0.86[CHD][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap]
rs2020213	0.86[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs2037757	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];0.91[YRI][hapmap]
rs2099476	0.96[CEU][hapmap];0.90[JPT][hapmap]
rs2217839	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs2252726	0.86[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs2573080	0.89[ASW][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.82[JPT][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs2573083	0.89[ASW][hapmap];0.83[CHB][hapmap];0.84[CHD][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap]
rs2573085	0.89[CHD][hapmap];0.82[JPT][hapmap];1.00[MKK][hapmap]
rs2573088	0.89[ASW][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.82[JPT][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs2695094	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs2695103	0.89[ASW][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];1.00[MKK][hapmap];0.92[YRI][hapmap]
rs2695111	0.89[CEU][hapmap];0.91[YRI][hapmap]
rs2695112	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.91[MEX][hapmap];0.88[TSI][hapmap];0.91[YRI][hapmap]
rs2695729	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2695735	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];0.88[TSI][hapmap];0.91[YRI][hapmap]
rs2695738	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs2695743	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2695744	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs2695745	0.91[YRI][hapmap]
rs2695746	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs2695747	0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs2695750	0.89[ASW][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.82[JPT][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs2695752	0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs3108453	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs3108476	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs3770051	1.00[CEU][hapmap];0.86[TSI][hapmap]
rs6433705	0.81[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs6743194	0.96[CEU][hapmap]
rs6745288	0.86[JPT][hapmap]
rs7573622	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs7604345	0.82[JPT][hapmap]
rs934807	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs959157	0.92[CEU][hapmap];0.86[CHD][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap]
rs959792	0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs966433	0.86[JPT][hapmap]

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	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875451	chr2:178748294-178953409	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv998304	chr2:178756380-178924378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536056	chr2:178756380-178924378	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv3055	chr2:178800438-178819638	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	esv2762296	chr2:178812726-178818029	Inactive region	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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