Variant report

Variant	rs7093036
Chromosome Location	chr10:26214247-26214248
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-5	chr10:26213307-26215945	NONHSAT011817

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10128266	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10128512	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10828903	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014826	1.00[AMR][1000 genomes]
rs11014835	1.00[AMR][1000 genomes]
rs11014836	1.00[AMR][1000 genomes]
rs11014838	1.00[AMR][1000 genomes]
rs11014843	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014844	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014849	0.88[AFR][1000 genomes]
rs11014858	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12249093	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12251038	1.00[AMR][1000 genomes]
rs12252281	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12254587	1.00[AMR][1000 genomes]
rs12255497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12258905	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12260850	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12267363	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58289791	1.00[AMR][1000 genomes]
rs7073840	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7086945	1.00[AMR][1000 genomes]
rs7086963	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7087106	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7089023	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7099128	1.00[AMR][1000 genomes]
rs7099929	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73610364	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73610365	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7904403	1.00[AMR][1000 genomes]
rs7905635	1.00[AMR][1000 genomes]
rs7911886	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7924004	1.00[AFR][1000 genomes];1.00[AMR][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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26212400-26215000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26214200-26214800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr10:26214200-26215400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:26214200-26215400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr10:26214200-26215400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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