Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10874912	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10874914	0.81[AMR][1000 genomes]
rs11165366	0.86[EUR][1000 genomes]
rs11165367	0.86[EUR][1000 genomes]
rs11165379	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12116466	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12118116	0.82[EUR][1000 genomes]
rs12135605	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12141215	0.82[EUR][1000 genomes]
rs12142805	0.89[EUR][1000 genomes]
rs12752448	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1548278	0.86[EUR][1000 genomes]
rs17589093	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2182021	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4359066	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4604740	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61771812	0.86[EUR][1000 genomes]
rs72723875	0.80[AMR][1000 genomes]
rs912648	0.86[EUR][1000 genomes]
rs927703	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[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	nsv830648	chr1:95760162-95926264	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1006113	chr1:95768502-96139003	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv529002	chr1:95781217-95805002	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95787600-95789800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:95787800-95790000	Enhancers	Brain Hippocampus Middle	brain
3	chr1:95788000-95790600	Weak transcription	Fetal Brain Female	brain
4	chr1:95788400-95791200	Enhancers	Brain Cingulate Gyrus	brain
5	chr1:95788600-95790600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:95789400-95790000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:95789400-95791800	Weak transcription	Brain Inferior Temporal Lobe	brain

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