Variant report

Variant	rs35546944
Chromosome Location	chr12:41203264-41203265
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12831625	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34031277	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34519483	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34552698	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34778624	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34797157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34862559	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35148802	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35234650	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35291059	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35319114	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35354319	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35489344	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs36063194	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58321893	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs66467974	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67410126	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71449780	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71449781	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71449782	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71449783	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427909	chr12:41054306-41322257	Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832379	chr12:41054440-41232749	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832380	chr12:41132306-41323961	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv469362	chr12:41155000-41206520	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv558697	chr12:41155000-41206520	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv469363	chr12:41155000-41214848	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv558698	chr12:41155000-41214848	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41201200-41203400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:41201400-41203600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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