Variant report

Variant	rs17175072
Chromosome Location	chr3:102724770-102724771
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs12630221	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12630253	0.94[ASN][1000 genomes]
rs12630685	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12630993	0.88[ASN][1000 genomes]
rs12632551	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12635938	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12636072	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12636511	0.88[ASN][1000 genomes]
rs12638685	0.94[ASN][1000 genomes]
rs17174940	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2125115	0.94[ASN][1000 genomes]
rs28379317	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28589342	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35529502	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55635015	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57767037	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58471102	0.92[ASN][1000 genomes]
rs58726139	0.94[ASN][1000 genomes]
rs59083363	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59536191	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60566616	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6779197	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6802674	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73136537	0.84[ASN][1000 genomes]
rs73141413	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73141416	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73141417	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73141425	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73149013	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73149293	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73149294	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73151190	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73151216	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73151220	0.94[ASN][1000 genomes]
rs73151224	0.94[ASN][1000 genomes]
rs73157435	0.88[ASN][1000 genomes]
rs73157438	0.88[ASN][1000 genomes]
rs73157440	0.88[ASN][1000 genomes]
rs73157447	0.88[ASN][1000 genomes]
rs7627438	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7634719	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7650097	0.88[ASN][1000 genomes]
rs7652587	0.88[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	nsv1007340	chr3:102108954-102725099	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv536676	chr3:102108954-102725099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv877228	chr3:102345638-102751470	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv591190	chr3:102345638-102946216	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv1000584	chr3:102358773-102923378	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv915978	chr3:102386795-102949530	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv460792	chr3:102467051-103087654	ZNF genes & repeats Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv591191	chr3:102467051-103087654	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102722200-102725200	Weak transcription	Adipose Nuclei	Adipose
2	chr3:102723600-102731400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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