Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10496631	1.00[CHB][hapmap]
rs10496633	1.00[CHB][hapmap]
rs11675400	1.00[CHB][hapmap]
rs11677559	1.00[CHB][hapmap]
rs11686392	1.00[CHB][hapmap]
rs11689672	1.00[CHB][hapmap]
rs11694708	1.00[CHB][hapmap]
rs1213971	1.00[CHB][hapmap]
rs1358669	1.00[CHB][hapmap]
rs1430251	1.00[CHB][hapmap]
rs1430268	1.00[CHB][hapmap]
rs1439131	1.00[CHB][hapmap]
rs17211596	1.00[CHB][hapmap]
rs17211765	1.00[CHB][hapmap]
rs17212475	1.00[CHB][hapmap]
rs17212552	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs17213071	1.00[CHB][hapmap]
rs17213092	1.00[CHB][hapmap]
rs17213203	1.00[CHB][hapmap]
rs17270902	1.00[CHB][hapmap]
rs17279088	1.00[CHB][hapmap]
rs17319680	1.00[CHB][hapmap]
rs17319771	1.00[CHB][hapmap]
rs17319827	1.00[CHB][hapmap]
rs17666092	1.00[CHB][hapmap]
rs17666152	1.00[CHB][hapmap]
rs17722007	1.00[CHB][hapmap]
rs17722506	1.00[CHB][hapmap]
rs17722749	1.00[CHB][hapmap]
rs2420554	1.00[CHB][hapmap]
rs2901195	1.00[CHB][hapmap]
rs4563225	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv874989	chr2:124892592-125176030	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:124925400-124928600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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