Variant report

Variant	rs66466321
Chromosome Location	chr14:97237078-97237079
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11623586	1.00[ASN][1000 genomes]
rs41443751	1.00[ASN][1000 genomes]
rs4900341	1.00[ASN][1000 genomes]
rs4900342	1.00[ASN][1000 genomes]
rs4905540	1.00[ASN][1000 genomes]
rs4905554	1.00[ASN][1000 genomes]
rs55676539	1.00[ASN][1000 genomes]
rs55841808	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55892024	1.00[ASN][1000 genomes]
rs55909735	1.00[ASN][1000 genomes]
rs55946529	1.00[ASN][1000 genomes]
rs55967054	1.00[ASN][1000 genomes]
rs56056633	1.00[ASN][1000 genomes]
rs56096836	1.00[ASN][1000 genomes]
rs56097548	1.00[ASN][1000 genomes]
rs56128300	1.00[ASN][1000 genomes]
rs7145138	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72708750	1.00[ASN][1000 genomes]
rs72708755	1.00[ASN][1000 genomes]
rs72708758	1.00[ASN][1000 genomes]
rs72708763	1.00[ASN][1000 genomes]
rs72708765	1.00[ASN][1000 genomes]
rs72708767	1.00[ASN][1000 genomes]
rs72708773	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72708797	1.00[ASN][1000 genomes]
rs8007776	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048302	chr14:97000845-97250538	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1041078	chr14:97001679-97279220	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv1050075	chr14:97004951-97279220	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr14:97230600-97238800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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