Variant report

Variant	rs8190620
Chromosome Location	chr10:26517053-26517054
allele	A/G
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]
rs7069695	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7072964	0.87[YRI][hapmap]
rs73594320	0.88[AFR][1000 genomes]
rs7898197	1.00[AFR][1000 genomes]
rs7913376	1.00[YRI][hapmap]
rs8190734	0.85[YRI][hapmap]
rs8190736	0.85[YRI][hapmap]
rs8190737	0.85[YRI][hapmap]
rs8190741	0.85[YRI][hapmap]
rs8190794	1.00[CEU][hapmap]

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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr10:26514600-26518400	Weak transcription	Brain Anterior Caudate	brain
2	chr10:26515800-26518800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr10:26516400-26517600	Strong transcription	Brain Germinal Matrix	brain

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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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