Variant report

Variant	rs995973
Chromosome Location	chr14:26027327-26027328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1033599	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1033600	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12434204	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12882376	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12894028	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1950445	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1950446	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1950447	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1950448	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1950450	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1951072	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1955878	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1955880	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1955882	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1955889	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2207566	0.90[EUR][1000 genomes]
rs28676371	0.90[EUR][1000 genomes]
rs4981599	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4983113	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7145678	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7152181	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8011455	0.89[AFR][1000 genomes]
rs8013460	0.88[AFR][1000 genomes]
rs8018144	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs926911	0.89[AMR][1000 genomes];0.93[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	nsv901519	chr14:25949277-26043929	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv430993	chr14:25976760-26097160	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	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	chr14:26025800-26027400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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