Variant report

Variant	rs62452831
Chromosome Location	chr7:14113001-14113002
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1158613	0.87[EUR][1000 genomes]
rs11765313	1.00[AMR][1000 genomes]
rs11768508	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11772231	1.00[AMR][1000 genomes]
rs11772295	1.00[AMR][1000 genomes]
rs12154297	1.00[AMR][1000 genomes]
rs12154307	1.00[AMR][1000 genomes]
rs12154599	1.00[AMR][1000 genomes]
rs16878042	1.00[AMR][1000 genomes]
rs17167735	1.00[AMR][1000 genomes]
rs17167741	1.00[AMR][1000 genomes]
rs17167742	1.00[AMR][1000 genomes]
rs17167773	1.00[AMR][1000 genomes]
rs17167791	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17167826	0.93[EUR][1000 genomes]
rs17167847	1.00[AMR][1000 genomes]
rs62452785	1.00[AMR][1000 genomes]
rs62452786	1.00[AMR][1000 genomes]
rs62452787	1.00[AMR][1000 genomes]
rs62452788	1.00[AMR][1000 genomes]
rs62452792	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62452794	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62452795	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62452797	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62452798	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62452801	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62452805	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62452829	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62452832	1.00[AMR][1000 genomes]
rs62452833	1.00[AMR][1000 genomes]
rs62452846	1.00[AMR][1000 genomes]
rs62454609	1.00[AMR][1000 genomes]
rs62454644	1.00[AMR][1000 genomes]
rs62454645	1.00[AMR][1000 genomes]
rs62454649	1.00[AMR][1000 genomes]
rs62454651	1.00[AMR][1000 genomes]
rs73054156	1.00[AMR][1000 genomes]
rs73057914	1.00[AMR][1000 genomes]
rs73057927	1.00[AMR][1000 genomes]
rs73059926	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73059973	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7349970	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1015312	chr7:14092753-14266917	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14112400-14114000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:14113000-14114200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:14113000-14115000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:14113000-14115400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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