Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:65168552..65171425-chr8:65171785..65174235,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11992818	0.86[EUR][1000 genomes]
rs1485486	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1485488	0.86[EUR][1000 genomes]
rs16930988	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16930997	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2054776	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2119184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2165251	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2220203	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2883910	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34215741	0.83[EUR][1000 genomes]
rs4515592	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4517161	0.86[EUR][1000 genomes]
rs4737667	0.86[EUR][1000 genomes]
rs4737668	0.83[EUR][1000 genomes]
rs66464473	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs66771575	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67315487	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6987428	0.87[EUR][1000 genomes]
rs755764	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7833101	0.86[EUR][1000 genomes]
rs936790	0.82[EUR][1000 genomes];0.82[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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65168400-65179000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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