Variant report

Variant	rs58922309
Chromosome Location	chr3:121115255-121115256
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs3218652	1.00[AMR][1000 genomes]
rs57745805	1.00[AMR][1000 genomes]
rs58297766	1.00[AMR][1000 genomes]
rs58338355	1.00[AMR][1000 genomes]
rs58466835	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58525071	1.00[AMR][1000 genomes]
rs58881799	1.00[AMR][1000 genomes]
rs59634035	1.00[AMR][1000 genomes]
rs60108064	1.00[AMR][1000 genomes]
rs60204652	1.00[AMR][1000 genomes]
rs61004683	1.00[AMR][1000 genomes]
rs61040872	1.00[AMR][1000 genomes]
rs61059986	1.00[AMR][1000 genomes]
rs72971952	1.00[AMR][1000 genomes]
rs72971955	1.00[AMR][1000 genomes]
rs73855356	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855359	1.00[AMR][1000 genomes]
rs73855360	1.00[AMR][1000 genomes]
rs73855361	1.00[AMR][1000 genomes]
rs73855375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855378	1.00[AMR][1000 genomes]
rs73855380	1.00[AMR][1000 genomes]
rs73855381	1.00[AMR][1000 genomes]
rs73855385	1.00[AMR][1000 genomes]
rs73855388	1.00[AMR][1000 genomes]
rs73855389	1.00[AMR][1000 genomes]
rs73855390	1.00[AMR][1000 genomes]
rs73855391	1.00[AMR][1000 genomes]
rs73855392	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73855394	1.00[AMR][1000 genomes]
rs73855395	1.00[AMR][1000 genomes]
rs73855396	1.00[AMR][1000 genomes]
rs73855397	1.00[AMR][1000 genomes]
rs73855399	1.00[AMR][1000 genomes]
rs73855400	1.00[AMR][1000 genomes]
rs73855402	1.00[AMR][1000 genomes]
rs73857903	1.00[AMR][1000 genomes]
rs73857906	1.00[AMR][1000 genomes]
rs73857907	1.00[AMR][1000 genomes]
rs73857909	1.00[AMR][1000 genomes]
rs73857910	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998555	chr3:120700604-121348015	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv829701	chr3:120935402-121115932	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv521397	chr3:120970900-121192350	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv591395	chr3:120970900-121501070	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv591396	chr3:120970900-121557533	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv591397	chr3:120977383-121505882	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv829702	chr3:121045793-121227975	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv591398	chr3:121046468-121154193	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv591399	chr3:121046468-121160369	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv591400	chr3:121070299-121339354	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv591401	chr3:121094592-121160369	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv999335	chr3:121100283-121408766	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 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	chr3:121093000-121117000	Weak transcription	Ovary	ovary

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