Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10036616	1.00[CHB][hapmap]
rs10059511	1.00[CHB][hapmap]
rs10066206	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10072473	1.00[CEU][hapmap]
rs10074267	1.00[CHB][hapmap]
rs10074385	1.00[CHB][hapmap]
rs10075210	1.00[CHB][hapmap]
rs10078205	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10476775	0.83[AMR][1000 genomes]
rs10476777	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10477000	1.00[CHB][hapmap]
rs11956353	1.00[CHB][hapmap]
rs13361115	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17112418	1.00[CEU][hapmap]
rs2216641	1.00[CEU][hapmap]
rs28480497	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3812003	1.00[CHB][hapmap]
rs3812004	1.00[CHB][hapmap]
rs6876258	1.00[CHB][hapmap]
rs6881068	1.00[CHB][hapmap]
rs6898736	1.00[CHB][hapmap]
rs7356721	1.00[CHB][hapmap]
rs73794390	1.00[AMR][1000 genomes]
rs7721901	1.00[AMR][1000 genomes]
rs9324713	1.00[AMR][1000 genomes];1.00[ASN][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	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	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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