Variant report

Variant	rs440385
Chromosome Location	chr3:120564338-120564339
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1806707	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2016491	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2016526	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2456273	0.89[ASN][1000 genomes]
rs2675548	0.85[ASN][1000 genomes]
rs2931069	0.89[ASN][1000 genomes]
rs2948182	0.89[ASN][1000 genomes]
rs2971381	0.89[ASN][1000 genomes]
rs2971384	0.89[ASN][1000 genomes]
rs373024	0.82[JPT][hapmap]
rs374128	0.89[ASN][1000 genomes]
rs380245	0.89[ASN][1000 genomes]
rs383218	0.89[ASN][1000 genomes]
rs386107	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs388112	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs391361	0.89[ASN][1000 genomes]
rs396521	0.89[ASN][1000 genomes]
rs399491	0.89[ASN][1000 genomes]
rs401023	0.89[ASN][1000 genomes]
rs401613	0.89[ASN][1000 genomes]
rs408561	0.89[ASN][1000 genomes]
rs409119	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs410498	0.89[ASN][1000 genomes]
rs412962	0.89[ASN][1000 genomes]
rs413401	0.89[ASN][1000 genomes]
rs415044	0.89[ASN][1000 genomes]
rs420103	0.89[ASN][1000 genomes]
rs431241	0.89[ASN][1000 genomes]
rs434559	0.83[CHB][hapmap]
rs444107	0.85[ASN][1000 genomes]
rs446065	0.89[ASN][1000 genomes]
rs505191	0.89[ASN][1000 genomes]
rs509890	0.83[CHB][hapmap]
rs530979	0.80[ASN][1000 genomes]
rs531876	0.80[ASN][1000 genomes]
rs538488	1.00[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs553011	0.89[ASN][1000 genomes]
rs553479	0.89[ASN][1000 genomes]
rs556346	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs559461	0.80[ASN][1000 genomes]
rs560420	0.89[ASN][1000 genomes]
rs563089	0.89[ASN][1000 genomes]
rs586820	0.88[ASN][1000 genomes]
rs587015	0.89[ASN][1000 genomes]
rs616353	0.89[ASN][1000 genomes]
rs617769	0.89[ASN][1000 genomes]
rs646244	0.89[ASN][1000 genomes]
rs668038	0.85[ASN][1000 genomes]
rs679016	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs688424	0.89[ASN][1000 genomes]
rs701997	0.89[ASN][1000 genomes]
rs701999	0.89[ASN][1000 genomes]
rs702004	0.89[ASN][1000 genomes]
rs836338	0.89[ASN][1000 genomes]
rs836339	0.88[ASN][1000 genomes]
rs836340	0.89[ASN][1000 genomes]
rs836341	0.89[ASN][1000 genomes]
rs836343	0.88[ASN][1000 genomes]
rs856895	0.89[ASN][1000 genomes]
rs864458	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007557	chr3:119892894-120764353	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv536706	chr3:119892894-120764353	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv869548	chr3:120320731-121076337	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv916869	chr3:120360281-120973169	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv877378	chr3:120381530-120606438	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1005396	chr3:120460741-120580319	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv829700	chr3:120469191-120675763	Strong transcription Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv1012541	chr3:120482402-120580319	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv1014477	chr3:120482402-120583166	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
10	nsv877380	chr3:120522716-120606438	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr3:120559200-120564800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:120562600-120564800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:120564200-120564600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:120564200-120565000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:120564200-120565400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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