Variant report

Variant	rs10259881
Chromosome Location	chr7:78612075-78612076
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1006818	0.89[CEU][hapmap];0.98[TSI][hapmap]
rs10224972	0.82[CHB][hapmap];0.84[GIH][hapmap]
rs10240536	0.83[CHB][hapmap]
rs10269689	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs10485926	0.83[CHB][hapmap]
rs1073416	0.90[CEU][hapmap];0.93[TSI][hapmap]
rs12113491	0.84[CEU][hapmap];0.98[TSI][hapmap]
rs12534480	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap]
rs12537793	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs13438061	0.83[CHB][hapmap]
rs13438576	0.83[CHB][hapmap]
rs1476106	0.89[CEU][hapmap];0.92[CHB][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.82[YRI][hapmap]
rs2006635	0.89[CEU][hapmap]
rs2078428	0.90[CEU][hapmap]
rs2109713	0.89[CEU][hapmap];0.93[TSI][hapmap]
rs2191724	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.85[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap]
rs2215546	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap]
rs2215547	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4730596	0.89[CEU][hapmap];0.92[CHB][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.98[TSI][hapmap];0.82[YRI][hapmap]
rs4730599	0.89[CEU][hapmap];0.98[TSI][hapmap]
rs4730601	0.89[CEU][hapmap];0.98[TSI][hapmap]
rs6466468	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs727652	0.89[CEU][hapmap]
rs763593	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7777825	0.90[YRI][hapmap]
rs7779315	0.89[CEU][hapmap]
rs7789063	0.89[CEU][hapmap]
rs7793390	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs7805367	0.89[CEU][hapmap];0.98[TSI][hapmap]
rs7809089	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs9692247	0.83[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv482826	chr7:78548319-78717605	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv471642	chr7:78548320-78717605	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv1374013	chr7:78612070-78612075	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv2441426	chr7:78612071-78612075	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv2374098	chr7:78612071-78612076	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78612000-78612600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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