Variant report

Variant	rs4842457
Chromosome Location	chr12:87800566-87800567
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10777039	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12422458	0.96[ASN][1000 genomes]
rs4360774	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4409920	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4491334	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4512935	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4630369	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4643150	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4842563	0.96[ASN][1000 genomes]
rs4842564	0.96[ASN][1000 genomes]
rs4842565	0.96[ASN][1000 genomes]
rs4842571	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55693604	0.96[ASN][1000 genomes]
rs55707841	0.96[ASN][1000 genomes]
rs55865225	0.96[ASN][1000 genomes]
rs56333727	0.96[ASN][1000 genomes]
rs57416479	0.96[ASN][1000 genomes]
rs58341223	0.96[ASN][1000 genomes]
rs60016330	0.96[ASN][1000 genomes]
rs60860693	0.96[ASN][1000 genomes]
rs66537815	0.96[ASN][1000 genomes]
rs67210764	0.96[ASN][1000 genomes]
rs67891841	0.96[ASN][1000 genomes]
rs7307618	0.96[ASN][1000 genomes]
rs7968573	0.96[ASN][1000 genomes]
rs7968713	0.96[ASN][1000 genomes]
rs7970629	0.96[ASN][1000 genomes]
rs9783446	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9971641	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9971644	0.81[EUR][1000 genomes];0.97[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	nsv430523	chr12:87757132-87865832	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv430525	chr12:87757132-87905532	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3329221	chr12:87785317-87833393	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87799400-87801200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:87799400-87801400	Enhancers	HMEC	breast
3	chr12:87799600-87801200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr12:87800200-87800800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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