Variant report

Variant	rs2060015
Chromosome Location	chr3:156573930-156573931
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:156573384..156575270-chr3:156577093..156579148,2	K562	blood:
2	chr3:156543142..156545627-chr3:156572642..156575012,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000197980	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10936038	0.81[EUR][1000 genomes]
rs10936043	0.82[ASN][1000 genomes]
rs11707914	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11709901	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11711674	0.80[EUR][1000 genomes]
rs11712111	0.91[ASN][1000 genomes]
rs12492968	0.83[EUR][1000 genomes]
rs12629380	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12634915	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12638253	0.91[ASN][1000 genomes]
rs13070271	0.84[ASN][1000 genomes]
rs13097325	0.80[EUR][1000 genomes]
rs13322318	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1384538	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1560415	0.81[EUR][1000 genomes]
rs1560416	0.81[EUR][1000 genomes]
rs17382070	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2321290	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2321292	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2321455	0.82[ASN][1000 genomes]
rs2874488	0.82[ASN][1000 genomes]
rs2874495	0.82[ASN][1000 genomes]
rs344087	0.82[ASN][1000 genomes]
rs34667021	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3910072	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs453219	0.84[ASN][1000 genomes]
rs4589888	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4680312	0.91[ASN][1000 genomes]
rs62275765	0.84[ASN][1000 genomes]
rs6441101	0.82[ASN][1000 genomes]
rs6765353	0.82[ASN][1000 genomes]
rs6780427	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7615304	0.82[ASN][1000 genomes]
rs7637701	0.89[ASN][1000 genomes]
rs7638330	0.82[ASN][1000 genomes]
rs7638625	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9812895	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9818684	0.83[EUR][1000 genomes]
rs9820830	0.81[EUR][1000 genomes]
rs9837038	0.98[ASN][1000 genomes]
rs9837271	0.81[EUR][1000 genomes]
rs9844054	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9847187	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9858158	0.91[ASN][1000 genomes]
rs9865905	0.89[ASN][1000 genomes]
rs9866373	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9867621	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9871817	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9875585	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9875688	0.87[ASN][1000 genomes]
rs9876010	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[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	nsv428745	chr3:156405054-156577840	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv877685	chr3:156444383-156611676	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
3	nsv829765	chr3:156568263-156718496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs2060015	LINC00886	cis	Stomach	GTEx
rs2060015	LINC00886	cis	Artery Aorta	GTEx
rs2060015	LINC00886	cis	Esophagus Muscularis	GTEx
rs2060015	LINC00886	cis	Artery Tibial	GTEx
rs2060015	LINC00886	cis	Adipose Subcutaneous	GTEx
rs2060015	LINC00886	cis	lung	GTEx
rs2060015	LINC00886	cis	Skin Sun Exposed Lower leg	GTEx
rs2060015	LINC00886	cis	Nerve Tibial	GTEx

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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