Variant report

Variant	rs4282959
Chromosome Location	chr11:101132938-101132939
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:101132696..101134898-chr11:101137456..101139610,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10791449	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1783747	0.81[EUR][1000 genomes]
rs1942839	0.95[AMR][1000 genomes]
rs1943758	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2156520	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4121760	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4144343	1.00[AMR][1000 genomes]
rs4237600	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4335511	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4351785	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4754008	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754744	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs528237	0.81[EUR][1000 genomes]
rs528399	0.90[AMR][1000 genomes]
rs538458	0.90[AMR][1000 genomes]
rs572915	0.81[AMR][1000 genomes]
rs606386	0.85[AMR][1000 genomes]
rs607699	0.85[AMR][1000 genomes]
rs6590841	0.90[AMR][1000 genomes]
rs6590842	1.00[AMR][1000 genomes]
rs7102599	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7104105	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs7110399	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7119902	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7128630	0.95[AMR][1000 genomes]
rs7342177	1.00[AMR][1000 genomes]
rs7342182	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7932597	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7942104	0.90[AMR][1000 genomes]
rs877627	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs948749	1.00[AMR][1000 genomes]
rs948891	0.95[AMR][1000 genomes]
rs948892	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv556131	chr11:100985777-101480017	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv530644	chr11:101010088-101486038	Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	esv2753322	chr11:101052790-101311790	Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv832247	chr11:101123483-101298787	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 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	chr11:101126400-101169400	Weak transcription	Ovary	ovary

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