Variant report

Variant	rs13327449
Chromosome Location	chr3:98724440-98724441
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:52)

rs_ID	r²[population]
rs10084679	0.83[AMR][1000 genomes]
rs12330381	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13094707	0.93[ASN][1000 genomes]
rs13317610	0.88[EUR][1000 genomes]
rs13318536	0.93[ASN][1000 genomes]
rs13318960	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13320266	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13320890	0.83[AMR][1000 genomes]
rs13327485	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2133575	0.80[ASN][1000 genomes]
rs2454687	0.80[ASN][1000 genomes]
rs2470884	0.80[ASN][1000 genomes]
rs28528154	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28637457	0.93[ASN][1000 genomes]
rs28650813	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28821579	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28883308	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28890260	1.00[AMR][1000 genomes]
rs34693680	0.93[ASN][1000 genomes]
rs56172805	0.88[EUR][1000 genomes]
rs6795351	0.80[ASN][1000 genomes]
rs72938540	0.86[EUR][1000 genomes]
rs7621508	0.80[ASN][1000 genomes]
rs9289696	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9289699	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9289700	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9810407	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9818215	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9819279	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9819309	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9828045	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9833945	0.83[AMR][1000 genomes]
rs9836437	0.88[EUR][1000 genomes]
rs9836915	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9838166	0.88[EUR][1000 genomes]
rs9838238	0.83[AMR][1000 genomes]
rs9839559	0.83[AMR][1000 genomes]
rs9842226	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9842555	1.00[AMR][1000 genomes]
rs9848335	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9848583	0.83[AMR][1000 genomes]
rs9850469	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9852537	0.83[AMR][1000 genomes]
rs9852889	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9859042	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9864010	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9870940	0.97[EUR][1000 genomes]
rs9872073	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9872301	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9879302	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9883751	0.88[EUR][1000 genomes]
rs996199	0.80[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	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription 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	17 gene(s)	inside rSNPs	diseases
3	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv877214	chr3:98445324-98738006	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv980100	chr3:98714787-98766962	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 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	chr3:98717200-98730600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr3:98717600-98729200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:98721800-98726200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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