Variant report

Variant	rs2919309
Chromosome Location	chr8:62186187-62186188
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:92538229..92539823-chr8:62186115..62187635,2	K562	blood:

Variant related genes	Relation type
ENSG00000245904	Chromatin interaction
ENSG00000133639	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs28460733	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2919304	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2919316	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2919317	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2919318	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2931287	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2931293	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2931296	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2931297	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978490	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2978516	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2978518	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2978526	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2978528	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2978551	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2978557	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978559	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978560	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2978561	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978562	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978563	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3864675	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3886396	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 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	chr8:62186000-62186600	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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