Variant report

Variant	rs7898281
Chromosome Location	chr10:26531131-26531132
allele	A/G
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:15)

rs_ID	r²[population]
rs58554934	0.90[AFR][1000 genomes]
rs58555760	1.00[AMR][1000 genomes]
rs7072964	1.00[AMR][1000 genomes]
rs7904959	0.90[AFR][1000 genomes]
rs8190682	1.00[AMR][1000 genomes]
rs8190723	1.00[AMR][1000 genomes]
rs8190734	1.00[AMR][1000 genomes]
rs8190736	1.00[AMR][1000 genomes]
rs8190737	1.00[AMR][1000 genomes]
rs8190738	1.00[AMR][1000 genomes]
rs8190741	1.00[AMR][1000 genomes]
rs8190751	1.00[AMR][1000 genomes]
rs8190763	1.00[AMR][1000 genomes]
rs8190785	1.00[AMR][1000 genomes]
rs8190816	1.00[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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26519200-26557800	Weak transcription	Brain Anterior Caudate	brain
2	chr10:26528200-26531600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:26528200-26532200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:26528600-26531200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr10:26528800-26531400	Weak 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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