Variant report

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs117393	0.83[CEU][hapmap]
rs12687951	0.83[CEU][hapmap]
rs12690297	0.83[CEU][hapmap]
rs17320928	0.83[CEU][hapmap]
rs2025092	1.00[CEU][hapmap]
rs2025093	0.84[CEU][hapmap]
rs369539	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs369919	0.83[CEU][hapmap]
rs370928	0.83[CEU][hapmap]
rs371681	0.84[CEU][hapmap]
rs376664	0.84[CEU][hapmap]
rs378620	0.83[CEU][hapmap]
rs382096	0.84[CEU][hapmap]
rs397580	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs397902	1.00[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs410901	1.00[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs415971	0.81[CEU][hapmap]
rs418001	0.89[YRI][hapmap]
rs419619	1.00[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs421001	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs426592	0.94[CEU][hapmap]
rs4323631	0.84[CEU][hapmap]
rs432650	1.00[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs440205	0.83[CEU][hapmap]
rs453810	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs4893309	0.83[CEU][hapmap]
rs5941049	0.83[CEU][hapmap]
rs5942149	0.94[YRI][hapmap]
rs5942150	0.89[YRI][hapmap]
rs5942151	0.89[YRI][hapmap]
rs5942157	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs5942158	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs5942163	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5942164	0.83[CEU][hapmap]
rs5942185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5942187	0.83[CEU][hapmap]
rs5984161	0.83[CEU][hapmap]
rs5984909	0.83[CEU][hapmap]
rs6522496	0.83[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432350	chrX:91158935-91590765	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv3435339	chrX:91427773-91539017	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv532885	chrX:91428554-92377178	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv533436	chrX:91434301-91519622	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:91464800-91467800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chrX:91464800-91469000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chrX:91466000-91468600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chrX:91466600-91467000	Enhancers	Hela-S3	cervix
5	chrX:91466600-91467800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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