Variant report

Variant	rs17314320
Chromosome Location	chr8:65199012-65199013
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10087386	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10090207	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10093773	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10097129	0.84[EUR][1000 genomes]
rs10097471	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10098936	0.80[EUR][1000 genomes]
rs10099867	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10103220	0.88[EUR][1000 genomes]
rs10104164	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10105633	0.85[EUR][1000 genomes]
rs10957306	0.89[EUR][1000 genomes]
rs12334830	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12335124	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12708021	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13252463	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13252892	0.86[EUR][1000 genomes]
rs13254698	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13262851	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13274668	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13275299	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1371684	0.90[EUR][1000 genomes]
rs1371685	0.90[EUR][1000 genomes]
rs1440135	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1440136	0.85[EUR][1000 genomes]
rs1440137	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16931063	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17223648	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17315206	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2008156	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2009633	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28631026	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28643545	0.87[EUR][1000 genomes]
rs28875492	0.83[EUR][1000 genomes]
rs28895626	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36058435	1.00[AFR][1000 genomes]
rs4478613	0.89[EUR][1000 genomes]
rs62521215	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62521216	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs67633283	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7822866	0.84[EUR][1000 genomes]
rs7841666	0.84[EUR][1000 genomes]
rs971236	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948343	chr8:64804219-65328394	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
3	nsv890971	chr8:65028814-65242166	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65198400-65199400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:65199000-65199400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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