Variant report

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

rs_ID	r²[population]
rs12555674	0.81[AFR][1000 genomes]
rs16923322	1.00[EUR][1000 genomes]
rs16923327	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16935847	1.00[EUR][1000 genomes]
rs16935854	1.00[EUR][1000 genomes]
rs16935858	1.00[EUR][1000 genomes]
rs16935873	1.00[EUR][1000 genomes]
rs16935914	0.81[AFR][1000 genomes]
rs16935921	0.81[YRI][hapmap]
rs56668669	0.84[AFR][1000 genomes]
rs60705810	1.00[EUR][1000 genomes]
rs6475164	1.00[EUR][1000 genomes]
rs7019508	0.86[YRI][hapmap]
rs7021598	1.00[EUR][1000 genomes]
rs7022381	1.00[EUR][1000 genomes]
rs7023310	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7037443	1.00[EUR][1000 genomes]
rs73645143	1.00[EUR][1000 genomes]
rs73645153	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73645154	0.87[AMR][1000 genomes]
rs7862608	1.00[EUR][1000 genomes]
rs7869947	0.83[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016971	chr9:17648242-17720176	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
2	nsv1021022	chr9:17649360-17723730	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
3	nsv892675	chr9:17694823-17790526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv466279	chr9:17699981-17726581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv613705	chr9:17699981-17726581	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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