Variant report

Variant	rs9649975
Chromosome Location	chr8:92656219-92656220
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1457052	0.92[EUR][1000 genomes]
rs28735086	0.85[EUR][1000 genomes]
rs56160120	0.92[EUR][1000 genomes]
rs56318259	0.89[EUR][1000 genomes]
rs57453564	0.85[EUR][1000 genomes]
rs57610492	0.81[EUR][1000 genomes]
rs58830410	0.85[EUR][1000 genomes]
rs58888435	0.89[EUR][1000 genomes]
rs59075912	0.92[EUR][1000 genomes]
rs73309604	0.85[EUR][1000 genomes]
rs73309653	0.89[EUR][1000 genomes]
rs73309657	0.89[EUR][1000 genomes]
rs73309674	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7832321	0.92[EUR][1000 genomes]

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	nsv1029962	chr8:92560661-92753342	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv831391	chr8:92578256-92761091	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92655800-92658200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:92655800-92658200	Enhancers	NHDF-Ad	bronchial
3	chr8:92655800-92658400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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