Variant report

Variant	rs73863014
Chromosome Location	chr3:135506773-135506774
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11916990	1.00[ASN][1000 genomes]
rs1401543	1.00[ASN][1000 genomes]
rs16843365	0.89[EUR][1000 genomes]
rs17195888	1.00[ASN][1000 genomes]
rs17196014	1.00[ASN][1000 genomes]
rs17196097	1.00[ASN][1000 genomes]
rs17249203	1.00[ASN][1000 genomes]
rs1878993	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2176666	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2895793	1.00[ASN][1000 genomes]
rs34629706	1.00[ASN][1000 genomes]
rs56380708	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56382648	1.00[ASN][1000 genomes]
rs56818259	1.00[ASN][1000 genomes]
rs57767257	0.89[EUR][1000 genomes]
rs57895104	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59165430	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs60349283	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60545022	1.00[ASN][1000 genomes]
rs61789012	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61789017	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61789024	0.89[EUR][1000 genomes]
rs61789025	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61789026	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790390	1.00[ASN][1000 genomes]
rs61790396	1.00[ASN][1000 genomes]
rs61790400	1.00[ASN][1000 genomes]
rs61790401	1.00[ASN][1000 genomes]
rs61790403	1.00[ASN][1000 genomes]
rs61790404	1.00[ASN][1000 genomes]
rs61790457	1.00[ASN][1000 genomes]
rs61790458	1.00[ASN][1000 genomes]
rs61790459	1.00[ASN][1000 genomes]
rs6414336	1.00[ASN][1000 genomes]
rs6762218	1.00[ASN][1000 genomes]
rs6765327	1.00[ASN][1000 genomes]
rs6769033	1.00[ASN][1000 genomes]
rs6769893	1.00[ASN][1000 genomes]
rs6786217	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6802942	1.00[ASN][1000 genomes]
rs72977660	1.00[ASN][1000 genomes]
rs73863035	1.00[ASN][1000 genomes]
rs7618257	1.00[ASN][1000 genomes]
rs7635010	1.00[ASN][1000 genomes]
rs908827	1.00[ASN][1000 genomes]
rs980210	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr3:135502000-135511200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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