Variant report

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

rs_ID	r²[population]
rs10036616	0.94[CEU][hapmap]
rs10059511	0.94[CEU][hapmap]
rs10062143	0.84[CEU][hapmap]
rs10066997	0.84[EUR][1000 genomes]
rs10074267	0.94[CEU][hapmap]
rs10074385	0.93[CEU][hapmap]
rs10075210	0.94[CEU][hapmap]
rs10079457	0.94[CEU][hapmap]
rs10477000	0.94[CEU][hapmap]
rs11956353	0.94[CEU][hapmap]
rs2913880	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913883	0.88[EUR][1000 genomes]
rs2913890	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2964602	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3812003	0.94[CEU][hapmap]
rs3812004	0.94[CEU][hapmap]
rs6876258	0.94[CEU][hapmap]
rs6881068	0.94[CEU][hapmap]
rs6898736	0.94[CEU][hapmap]
rs7356721	0.94[CEU][hapmap]
rs7709656	0.84[EUR][1000 genomes]
rs9324715	0.82[EUR][1000 genomes]

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	esv1808837	chr5:151238149-151260215	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3487128	chr5:151247859-151254357	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3487127	chr5:151248309-151254207	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3487129	chr5:151248309-151254207	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3471107	chr5:151249859-151254957	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151235200-151264200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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