Variant report

Variant	rs12632522
Chromosome Location	chr3:140238918-140238919
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10513115	0.84[ASN][1000 genomes]
rs12629444	0.84[ASN][1000 genomes]
rs12629920	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12630402	0.84[ASN][1000 genomes]
rs12630595	0.94[ASN][1000 genomes]
rs12632435	0.83[ASN][1000 genomes]
rs12633853	0.87[ASN][1000 genomes]
rs12634135	0.84[ASN][1000 genomes]
rs12637306	0.84[ASN][1000 genomes]
rs12637548	0.84[ASN][1000 genomes]
rs12639333	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12639367	0.84[ASN][1000 genomes]
rs12639449	0.81[ASN][1000 genomes]
rs12639512	0.84[ASN][1000 genomes]
rs12639527	0.84[ASN][1000 genomes]
rs12639548	0.84[ASN][1000 genomes]
rs17415202	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2081804	0.88[ASN][1000 genomes]
rs28855402	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28896542	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55745214	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55905797	0.84[ASN][1000 genomes]
rs55955749	0.84[ASN][1000 genomes]
rs56055908	0.84[ASN][1000 genomes]
rs56144656	0.84[ASN][1000 genomes]
rs56162844	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56167447	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56178346	0.84[ASN][1000 genomes]
rs56205320	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59359471	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73231210	0.83[ASN][1000 genomes]
rs73231212	0.83[ASN][1000 genomes]
rs73231213	0.84[ASN][1000 genomes]
rs73231214	0.81[ASN][1000 genomes]
rs73231215	0.84[ASN][1000 genomes]
rs73231216	0.84[ASN][1000 genomes]
rs73231219	0.84[ASN][1000 genomes]
rs73231221	0.84[ASN][1000 genomes]
rs73231225	0.84[ASN][1000 genomes]
rs73231228	0.88[ASN][1000 genomes]
rs73231230	0.94[ASN][1000 genomes]
rs73231231	0.94[ASN][1000 genomes]
rs73231241	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73231242	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73231244	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73231248	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73231252	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7614244	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7618181	0.88[ASN][1000 genomes]
rs8179950	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757891	chr3:139925764-140524730	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759181	chr3:139925764-140524730	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv527831	chr3:139932966-140533823	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv34489	chr3:140009020-140469302	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv2757012	chr3:140009220-140460228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv591863	chr3:140126067-140274442	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140224400-140247200	Weak transcription	Ovary	ovary
2	chr3:140227400-140240800	Weak transcription	HSMMtube	muscle
3	chr3:140230000-140240000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr3:140237200-140240200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:140237400-140249400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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