Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10444685	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10444741	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs11625620	1.00[ASN][1000 genomes]
rs11625769	1.00[ASN][1000 genomes]
rs12147236	1.00[ASN][1000 genomes]
rs12147614	1.00[ASN][1000 genomes]
rs17836166	1.00[ASN][1000 genomes]
rs61519036	1.00[ASN][1000 genomes]
rs61993116	1.00[ASN][1000 genomes]
rs61993137	1.00[ASN][1000 genomes]
rs61993138	1.00[ASN][1000 genomes]
rs61993139	1.00[ASN][1000 genomes]
rs61993140	1.00[ASN][1000 genomes]
rs61993141	1.00[ASN][1000 genomes]
rs61993159	1.00[ASN][1000 genomes]
rs61995163	1.00[ASN][1000 genomes]
rs61995166	1.00[ASN][1000 genomes]
rs61995177	1.00[ASN][1000 genomes]
rs61995185	1.00[ASN][1000 genomes]
rs7145128	0.96[CEU][hapmap];0.92[EUR][1000 genomes]
rs7150181	0.82[CEU][hapmap]
rs8005235	0.88[CEU][hapmap];0.87[YRI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8021408	0.92[CEU][hapmap];1.00[YRI][hapmap]
rs8022132	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv902112	chr14:79939393-80050771	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79961400-79961800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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