Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10736431	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10890566	0.85[AFR][1000 genomes]
rs10890568	0.99[ASN][1000 genomes]
rs11211878	0.84[ASN][1000 genomes]
rs11211880	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11211884	0.82[ASN][1000 genomes]
rs11823116	0.82[ASN][1000 genomes]
rs12420232	0.85[AFR][1000 genomes]
rs1487903	0.82[ASN][1000 genomes]
rs1938622	0.82[ASN][1000 genomes]
rs2220376	0.81[ASN][1000 genomes]
rs3907374	0.82[ASN][1000 genomes]
rs4121676	0.81[ASN][1000 genomes]
rs4409792	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4423153	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4528295	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4533009	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4754166	0.81[EUR][1000 genomes]
rs6588917	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6588921	0.82[ASN][1000 genomes]
rs7128815	0.80[ASN][1000 genomes]
rs7931295	0.83[EUR][1000 genomes]
rs7933195	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv898359	chr11:106523574-106656863	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv898360	chr11:106566114-106598286	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv898361	chr11:106567910-106598286	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106552800-106628200	Weak transcription	Pancreas	Pancrea
2	chr11:106554800-106585000	Weak transcription	Fetal Lung	lung
3	chr11:106577600-106585200	Weak transcription	NH-A	brain
4	chr11:106583400-106583800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr11:106583400-106595800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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