Variant report

Variant	rs34358304
Chromosome Location	chr6:118332160-118332161
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs13198431	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13211121	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1338971	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17079625	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2211099	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2355798	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34729097	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs36172496	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4113075	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4120871	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4245490	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4434501	0.87[AMR][1000 genomes]
rs4945604	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4946312	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5002415	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6914871	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6928714	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6935258	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7744988	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9374693	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9374698	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9387532	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9401043	0.92[AMR][1000 genomes]
rs9401045	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9481751	0.84[EUR][1000 genomes]
rs9489290	0.83[EUR][1000 genomes]
rs9766457	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9968789	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 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	chr6:118323400-118332800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:118324800-118332600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:118329600-118332800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:118332000-118332200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:118332000-118332600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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