Variant report

Variant	rs7447610
Chromosome Location	chr5:95605114-95605115
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10062171	0.85[ASN][1000 genomes]
rs10064683	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10213951	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10476546	0.91[YRI][hapmap]
rs10476668	0.80[ASN][1000 genomes]
rs11135450	0.91[YRI][hapmap]
rs12518407	0.85[ASN][1000 genomes]
rs12518754	0.80[ASN][1000 genomes]
rs12521786	0.80[ASN][1000 genomes]
rs271920	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs271922	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs271924	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs271925	0.83[CHB][hapmap]
rs271926	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs28788264	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4077816	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4264961	0.82[AMR][1000 genomes]
rs4283814	0.80[ASN][1000 genomes]
rs4367317	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4379224	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4464721	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4502854	0.80[ASN][1000 genomes]
rs4635954	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4635955	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4869275	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4869279	0.80[ASN][1000 genomes]
rs55745974	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56311820	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6233	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs62366027	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62366031	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6556912	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6876484	0.80[ASN][1000 genomes]
rs6881060	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6881916	0.80[ASN][1000 genomes]
rs6885381	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6888535	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6893547	0.88[CHB][hapmap]
rs6895341	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6899076	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72787618	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7448311	0.80[ASN][1000 genomes]
rs7708068	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv830410	chr5:95505799-95666310	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr5:95595400-95614800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:95604600-95605200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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