Variant report

Variant	rs700726
Chromosome Location	chr8:60931328-60931329
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:60928178..60929748-chr8:60930851..60932873,2	K562	blood:
2	chr8:60929909..60932479-chr8:60938404..60940502,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1626773	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2622526	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2688656	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs475714	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs488934	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs490409	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs493713	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs497312	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs507158	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs510005	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs519500	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs533776	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs544344	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs544416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs548902	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs549730	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs574368	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs574929	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs594035	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs595330	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs595819	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs598457	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs627807	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs642072	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs648946	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs649886	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs659506	0.86[EUR][1000 genomes]
rs666087	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs668563	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs671655	0.81[AMR][1000 genomes];0.83[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	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv968509	chr8:60926652-60932214	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60930600-60932200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:60931200-60932600	Enhancers	Fetal Lung	lung

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