Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10219285	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11031799	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11031800	0.97[EUR][1000 genomes]
rs11031801	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11031813	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12271863	0.97[EUR][1000 genomes]
rs12276814	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12277550	0.91[EUR][1000 genomes]
rs12282084	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12789194	0.90[EUR][1000 genomes]
rs12789525	0.80[EUR][1000 genomes]
rs12790633	0.91[EUR][1000 genomes]
rs12794418	0.95[EUR][1000 genomes]
rs12798270	0.89[EUR][1000 genomes]
rs12805730	0.92[EUR][1000 genomes]
rs12808723	0.93[EUR][1000 genomes]
rs17748371	0.87[EUR][1000 genomes]
rs35128594	0.88[EUR][1000 genomes]
rs35245711	0.91[EUR][1000 genomes]
rs7105159	0.88[ASN][1000 genomes]
rs7115617	0.95[EUR][1000 genomes]
rs7118228	0.83[EUR][1000 genomes]
rs9300011	0.97[EUR][1000 genomes]
rs9300012	0.97[EUR][1000 genomes]
rs9300013	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9651595	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv2753303	chr11:32447324-32494924	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32469000-32487800	Weak transcription	Ovary	ovary
2	chr11:32475200-32487600	Weak transcription	Fetal Kidney	kidney
3	chr11:32483000-32484600	Enhancers	Fetal Muscle Leg	muscle

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