Variant report

Variant	rs8190794
Chromosome Location	chr10:26589132-26589133
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs74126409	0.84[AMR][1000 genomes]
rs8190620	1.00[CEU][hapmap]
rs8190798	0.84[AMR][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	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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26583600-26591000	Weak transcription	Brain Anterior Caudate	brain
2	chr10:26586800-26594600	Weak transcription	Fetal Brain Female	brain
3	chr10:26587400-26599000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr10:26587800-26589600	Enhancers	Fetal Lung	lung
5	chr10:26587800-26590600	Weak transcription	Brain Germinal Matrix	brain
6	chr10:26589000-26590000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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