Variant report

Variant	rs61789012
Chromosome Location	chr3:135473945-135473946
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11916990	1.00[ASN][1000 genomes]
rs1401543	1.00[ASN][1000 genomes]
rs16843365	0.85[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	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2176666	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2895793	1.00[ASN][1000 genomes]
rs56380708	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56382648	1.00[ASN][1000 genomes]
rs56818259	1.00[ASN][1000 genomes]
rs57767257	0.85[EUR][1000 genomes]
rs57895104	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59165430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60349283	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60545022	1.00[ASN][1000 genomes]
rs61789017	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61789024	0.85[EUR][1000 genomes]
rs61789025	1.00[ASN][1000 genomes]
rs61789026	0.83[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	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72977660	1.00[ASN][1000 genomes]
rs73863014	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135451200-135482000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:135473400-135476000	Enhancers	Fetal Brain Female	brain
3	chr3:135473400-135476200	Enhancers	Fetal Brain Male	brain
4	chr3:135473600-135474200	Weak transcription	Brain Germinal Matrix	brain

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