Variant report

Variant	rs1433585
Chromosome Location	chr8:130626097-130626098
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11785889	0.81[EUR][1000 genomes]
rs12681229	0.94[CEU][hapmap]
rs1583333	0.87[CEU][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs16904121	0.80[CEU][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs16904123	0.87[CEU][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs16904126	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16904129	0.93[CEU][hapmap];0.86[GIH][hapmap];0.84[MEX][hapmap];0.82[TSI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1946627	0.83[EUR][1000 genomes]
rs4487716	0.83[EUR][1000 genomes]
rs58811566	0.83[EUR][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	nsv612230	chr8:130624121-130661901	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	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	chr8:130626000-130626200	Enhancers	Fetal Lung	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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