Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17077783	0.93[EUR][1000 genomes]
rs56742355	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61318536	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs66460106	0.85[AMR][1000 genomes]
rs66697853	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67213527	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67896489	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7324310	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9531553	0.85[AMR][1000 genomes]
rs9531555	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9531557	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9531558	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9546592	0.85[AMR][1000 genomes]
rs9546602	0.87[AMR][1000 genomes]
rs9546612	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9546613	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9546614	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9546615	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9546616	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9546617	0.85[AMR][1000 genomes]
rs9546618	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9546621	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][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	nsv1046982	chr13:84631965-84800765	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1038880	chr13:84632431-84861839	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv949402	chr13:84675752-85606846	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1035493	chr13:84683545-84779862	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv900687	chr13:84691001-84714655	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv562557	chr13:84695884-84714655	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv1044494	chr13:84705200-84897141	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:84705600-84710200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr13:84705600-84711000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:84705600-84713000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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