Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:127879946..127881512-chr4:127913269..127915324,2	K562	blood:

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

rs_ID	r²[population]
rs10022263	0.91[ASN][1000 genomes]
rs13141365	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13142099	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13147915	0.91[ASN][1000 genomes]
rs1397437	0.91[ASN][1000 genomes]
rs1510687	0.87[ASN][1000 genomes]
rs1510688	0.87[ASN][1000 genomes]
rs17011892	0.86[ASN][1000 genomes]
rs1848934	0.87[ASN][1000 genomes]
rs2221773	0.91[ASN][1000 genomes]
rs28376541	0.87[ASN][1000 genomes]
rs28706560	0.91[ASN][1000 genomes]
rs28881307	0.91[ASN][1000 genomes]
rs28883271	0.91[ASN][1000 genomes]
rs340439	0.85[ASN][1000 genomes]
rs340440	0.85[ASN][1000 genomes]
rs36069962	0.91[ASN][1000 genomes]
rs62324472	0.86[ASN][1000 genomes]
rs6821583	0.87[ASN][1000 genomes]
rs6821961	0.87[ASN][1000 genomes]
rs7686658	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[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	nsv830055	chr4:127794875-127993821	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv879913	chr4:127844803-127948196	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv1006673	chr4:127913488-127915493	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127912600-127914800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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