Variant report

Variant	rs671372
Chromosome Location	chr7:103372911-103372912
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs13239238	0.81[ASN][1000 genomes]
rs2237633	0.81[ASN][1000 genomes]
rs2299377	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2299378	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2299379	0.86[AMR][1000 genomes]
rs2299380	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35441390	0.81[ASN][1000 genomes]
rs36011270	0.81[ASN][1000 genomes]
rs473940	0.94[ASN][1000 genomes]
rs477444	0.94[ASN][1000 genomes]
rs478549	0.85[CEU][hapmap];0.94[ASN][1000 genomes]
rs495374	0.89[ASN][1000 genomes]
rs496535	0.80[EUR][1000 genomes]
rs507226	0.94[ASN][1000 genomes]
rs512529	0.93[ASN][1000 genomes]
rs525692	0.93[ASN][1000 genomes]
rs528528	0.81[CEU][hapmap];0.94[ASN][1000 genomes]
rs531330	0.83[CEU][hapmap];0.94[ASN][1000 genomes]
rs541768	0.85[CEU][hapmap];0.89[ASN][1000 genomes]
rs562393	0.94[ASN][1000 genomes]
rs562444	0.94[ASN][1000 genomes]
rs570418	0.83[CEU][hapmap];0.94[ASN][1000 genomes]
rs571990	0.83[CEU][hapmap];0.94[ASN][1000 genomes]
rs607755	0.82[CEU][hapmap];0.92[ASN][1000 genomes]
rs618925	0.87[ASN][1000 genomes]
rs620243	0.85[CEU][hapmap];0.94[ASN][1000 genomes]
rs620774	0.89[ASN][1000 genomes]
rs621223	0.83[CEU][hapmap];0.94[ASN][1000 genomes]
rs621311	0.91[ASN][1000 genomes]
rs622657	0.85[CEU][hapmap];0.94[ASN][1000 genomes]
rs62480700	0.88[ASN][1000 genomes]
rs626065	0.80[EUR][1000 genomes]
rs637577	0.94[ASN][1000 genomes]
rs637606	0.94[ASN][1000 genomes]
rs637872	0.80[EUR][1000 genomes]
rs651097	0.82[CEU][hapmap];0.92[ASN][1000 genomes]
rs682507	0.94[ASN][1000 genomes]
rs683390	0.82[CEU][hapmap];0.93[ASN][1000 genomes]
rs6953960	0.85[CEU][hapmap];0.95[ASN][1000 genomes]
rs7780986	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 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	chr7:103355400-103374800	Weak transcription	HepG2	liver
2	chr7:103371800-103374200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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