Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:110656736..110659365-chr9:110662129..110664911,2	K562	blood:

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

rs_ID	r²[population]
rs10448248	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10512377	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10979082	0.83[AMR][1000 genomes]
rs10979087	0.90[AMR][1000 genomes]
rs10979088	0.90[AMR][1000 genomes]
rs10979089	0.87[AMR][1000 genomes]
rs10979094	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10979095	0.97[EUR][1000 genomes]
rs10979096	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10979097	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10979098	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10979102	0.97[EUR][1000 genomes]
rs10979103	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10979105	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10979106	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10979109	0.95[EUR][1000 genomes]
rs12376697	0.95[EUR][1000 genomes]
rs12377933	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12379423	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12380068	0.87[ASN][1000 genomes]
rs1888615	0.80[EUR][1000 genomes]
rs2210328	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34048749	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][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	nsv1051101	chr9:110548257-110697253	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv893701	chr9:110650482-110709587	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110658000-110668000	Weak transcription	Placenta	Placenta
2	chr9:110661600-110670000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:110661800-110666800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr9:110662200-110667600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:110664000-110667000	Weak transcription	Primary B cells from cord blood	blood

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