Variant report

Variant	rs17665266
Chromosome Location	chr10:26125288-26125289
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10508707	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12771482	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12771652	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12777505	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12780444	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16926410	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34144304	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35316154	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36001363	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71495483	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs71495484	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71495485	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs752740	1.00[AMR][1000 genomes];1.00[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	nsv894974	chr10:26028530-26322783	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1051756	chr10:26092320-26277478	Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:26124800-26125600	Bivalent Enhancer	Fetal Brain Male	brain
2	chr10:26125200-26125400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr10:26125200-26127200	Enhancers	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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