Variant report

Variant	rs7638246
Chromosome Location	chr3:52198322-52198323
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs123681	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12386365	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13314125	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13319566	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs164638	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs164639	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17051957	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17051977	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs171294	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs183029	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2304505	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28452586	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28659792	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352146	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352147	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352148	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352149	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352150	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352151	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352153	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55664415	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55834589	0.81[EUR][1000 genomes]
rs56281986	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56322622	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57335685	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57466127	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59890038	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6781635	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72964042	0.83[ASN][1000 genomes]
rs72964044	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs808787	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs876782	0.90[EUR][1000 genomes]
rs893056	0.87[EUR][1000 genomes]
rs9809254	0.87[EUR][1000 genomes]
rs9809977	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9811707	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9815010	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9816434	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9817653	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9830293	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9841469	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9843299	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9843852	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9846049	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9847073	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9847092	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9857878	0.87[EUR][1000 genomes]
rs9860982	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9868101	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9882775	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519445	chr3:52004317-52367932	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv876786	chr3:52041566-52236762	Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv984541	chr3:52055970-52285682	Genic enhancers Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv470572	chr3:52123313-52350212	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	103 gene(s)	inside rSNPs	diseases
5	nsv460537	chr3:52148233-52290550	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv590301	chr3:52148233-52290550	Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv508218	chr3:52155869-52290410	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
8	nsv834694	chr3:52178983-52335821	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	102 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52196200-52210400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:52196800-52200000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr3:52196800-52201200	Weak transcription	HepG2	liver

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