Variant report

Variant	rs12114187
Chromosome Location	chr8:63644834-63644835
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16929324	0.83[EUR][1000 genomes]
rs16929380	0.89[EUR][1000 genomes]
rs16929409	0.82[EUR][1000 genomes]
rs16929428	0.81[EUR][1000 genomes]
rs2127563	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs59113187	0.89[EUR][1000 genomes]
rs60508325	0.89[EUR][1000 genomes]
rs7016043	0.82[EUR][1000 genomes]
rs73682630	0.94[EUR][1000 genomes]
rs73682631	0.81[EUR][1000 genomes]
rs73683352	0.88[EUR][1000 genomes]
rs9969432	0.88[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	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831340	chr8:63515126-63702660	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63640800-63648200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:63644400-63648400	Weak transcription	H9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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