Variant report

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

rs_ID	r²[population]
rs10494927	1.00[AFR][1000 genomes]
rs1110266	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12126727	1.00[CHB][hapmap]
rs12354080	1.00[CHB][hapmap]
rs17188395	1.00[AFR][1000 genomes]
rs17188409	1.00[AFR][1000 genomes]
rs17188423	1.00[AFR][1000 genomes]
rs17188430	1.00[AFR][1000 genomes]
rs17188437	1.00[AFR][1000 genomes]
rs17188451	1.00[AFR][1000 genomes]
rs17188472	1.00[AFR][1000 genomes]
rs17188513	1.00[AFR][1000 genomes]
rs17260592	1.00[AFR][1000 genomes]
rs17260606	1.00[AFR][1000 genomes]
rs17260620	1.00[AFR][1000 genomes]
rs17260634	1.00[AFR][1000 genomes]
rs17260662	1.00[AFR][1000 genomes]
rs17260683	1.00[AFR][1000 genomes]
rs17260704	1.00[AFR][1000 genomes]
rs35376815	1.00[AFR][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	nsv832503	chr1:210948760-211103163	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211016000-211017200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr1:211016400-211017200	Strong transcription	HSMM	muscle
3	chr1:211016400-211024200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:211016600-211023400	Weak transcription	Brain Anterior Caudate	brain

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