Variant report

No.	Distal block	Cell Line	Cell type
1	chr10:23287418..23289094-chr10:23304568..23306972,2	K562	blood:
2	chr10:23303236..23310250-chr10:23341340..23346193,13	K562	blood:
3	chr10:23302995..23309769-chr10:23341340..23346193,8	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1054052	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1060761	0.80[AMR][1000 genomes]
rs10764371	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10764374	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10828394	0.82[AMR][1000 genomes]
rs10828396	0.90[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10828397	0.94[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10828400	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11013228	0.85[AMR][1000 genomes]
rs11013240	0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11013242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11013244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1170929	0.80[AMR][1000 genomes]
rs11814322	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12780334	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2219797	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4748833	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs58091240	0.90[AMR][1000 genomes]
rs6482247	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6482249	0.92[AMR][1000 genomes]
rs7901137	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[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	nsv975810	chr10:23302287-23306366	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23301400-23311200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr10:23304000-23305400	Enhancers	K562	blood
3	chr10:23304600-23305000	Enhancers	Primary B cells from peripheral blood	blood
4	chr10:23304600-23305400	Enhancers	GM12878-XiMat	blood

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