Variant report

Variant	rs58024273
Chromosome Location	chr12:86567539-86567540
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	chr12:86559122..86560912-chr12:86565276..86567562,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs12305255	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12306726	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1389296	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17284129	0.81[EUR][1000 genomes]
rs17284624	0.80[EUR][1000 genomes]
rs17284820	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17357025	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17359446	0.84[AMR][1000 genomes]
rs4586245	0.84[EUR][1000 genomes]
rs4842541	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55832610	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55886852	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55998036	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56154427	0.84[EUR][1000 genomes]
rs57624840	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59623111	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61931157	0.81[EUR][1000 genomes]
rs61932264	0.84[EUR][1000 genomes]
rs61932265	0.84[EUR][1000 genomes]
rs61932266	0.84[EUR][1000 genomes]
rs61932268	0.84[EUR][1000 genomes]
rs61932269	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61932270	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61932271	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61932272	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61932274	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61932275	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61948967	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61948994	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61949011	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61949013	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61949036	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61949037	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61949038	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61949039	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61949041	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61949045	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61949047	0.81[AMR][1000 genomes]
rs61949048	0.83[AMR][1000 genomes]
rs61949049	0.83[AMR][1000 genomes]
rs61950663	0.83[AMR][1000 genomes]
rs61950665	0.83[AMR][1000 genomes]
rs7487426	0.84[EUR][1000 genomes]
rs767898	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3442004	chr12:86514695-86599965	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	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	chr12:86566800-86568200	Enhancers	Fetal Heart	heart

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