Variant report

Variant	rs711709
Chromosome Location	chr3:22997652-22997653
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:22997497..23000412-chr3:23001550..23003702,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1671868	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1671884	0.87[EUR][1000 genomes]
rs1683074	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1708146	0.87[EUR][1000 genomes]
rs3914284	0.86[EUR][1000 genomes]
rs4858467	0.97[EUR][1000 genomes]
rs62252313	0.88[EUR][1000 genomes]
rs696492	0.84[EUR][1000 genomes]
rs696501	0.86[EUR][1000 genomes]
rs696502	0.83[EUR][1000 genomes]
rs696503	0.85[EUR][1000 genomes]
rs696504	0.84[EUR][1000 genomes]
rs696508	0.88[EUR][1000 genomes]
rs696509	0.87[EUR][1000 genomes]
rs697025	0.88[AMR][1000 genomes]
rs697026	0.88[AMR][1000 genomes]
rs698224	0.86[EUR][1000 genomes]
rs698228	0.84[EUR][1000 genomes]
rs698232	0.86[EUR][1000 genomes]
rs698235	0.90[AMR][1000 genomes]
rs698239	0.89[AMR][1000 genomes]
rs711698	0.86[EUR][1000 genomes]
rs711699	0.84[EUR][1000 genomes]
rs711704	0.95[EUR][1000 genomes]
rs711707	0.97[EUR][1000 genomes]
rs711708	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs711713	0.90[AMR][1000 genomes]
rs822204	0.83[CEU][hapmap];0.88[AMR][1000 genomes]
rs822754	0.88[EUR][1000 genomes]
rs822756	0.87[EUR][1000 genomes]
rs822757	0.86[EUR][1000 genomes]
rs822758	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs822779	0.97[EUR][1000 genomes]
rs822781	0.97[EUR][1000 genomes]
rs822783	0.97[EUR][1000 genomes]
rs822784	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs822785	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs822786	0.97[EUR][1000 genomes]
rs822787	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs822788	0.97[EUR][1000 genomes]
rs822789	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs822791	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1008306	chr3:22762892-23026548	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv998236	chr3:22979632-23011352	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22993400-23000800	Weak transcription	Fetal Lung	lung
2	chr3:22997200-22998600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:22997400-23001200	Weak transcription	Aorta	Aorta

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