Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10250078	1.00[AMR][1000 genomes]
rs10953437	1.00[YRI][hapmap]
rs12111933	1.00[AMR][1000 genomes]
rs1468861	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs1468862	1.00[YRI][hapmap]
rs1861610	1.00[AMR][1000 genomes]
rs2193199	1.00[AMR][1000 genomes]
rs2470962	1.00[AMR][1000 genomes]
rs4431535	1.00[AMR][1000 genomes]
rs4623345	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs4727610	1.00[YRI][hapmap]
rs4730033	1.00[AMR][1000 genomes]
rs4730046	1.00[AMR][1000 genomes]
rs6944590	1.00[AMR][1000 genomes]
rs6955297	1.00[YRI][hapmap]
rs6958342	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6979378	1.00[YRI][hapmap]
rs7784639	1.00[AMR][1000 genomes]
rs7801079	1.00[AMR][1000 genomes]
rs7801340	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429790	chr7:104314049-104488049	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr7:104338400-104342800	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:104341800-104343800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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