Variant report

Variant	rs7785985
Chromosome Location	chr7:80044796-80044797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10224553	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10227661	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10246082	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10260212	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10262631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10954165	0.98[EUR][1000 genomes]
rs10954166	0.98[EUR][1000 genomes]
rs17153872	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17153884	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17153898	0.94[EUR][1000 genomes]
rs28436901	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28692526	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4563825	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs471683	0.98[EUR][1000 genomes]
rs471775	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs483336	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs492403	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs496617	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs496621	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs496894	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs503046	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs504899	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs511060	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512689	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs513740	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs526183	0.98[EUR][1000 genomes]
rs526322	0.97[EUR][1000 genomes]
rs531197	0.98[EUR][1000 genomes]
rs533267	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534997	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs540192	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs552739	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs553993	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs562467	0.98[EUR][1000 genomes]
rs565166	0.98[EUR][1000 genomes]
rs565829	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs568125	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs570687	0.98[EUR][1000 genomes]
rs573316	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs575195	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57684477	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs577808	0.98[EUR][1000 genomes]
rs581101	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7784820	0.98[EUR][1000 genomes]
rs7785386	0.98[EUR][1000 genomes]
rs7790369	0.95[EUR][1000 genomes]
rs7792680	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7792890	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799056	0.98[EUR][1000 genomes]
rs7800677	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7808977	0.98[EUR][1000 genomes];1.00[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	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
2	nsv831042	chr7:79984079-80122312	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv464603	chr7:80030601-80064727	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607679	chr7:80030601-80064727	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1030961	chr7:80032525-80197468	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv538991	chr7:80032525-80197468	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1031915	chr7:80032898-80087603	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv949205	chr7:80039695-80211200	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80034200-80060200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:80042400-80044800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr7:80042800-80044800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:80043800-80045200	Enhancers	HMEC	breast
5	chr7:80044400-80044800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:80044400-80045200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:80044600-80044800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:80044600-80044800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:80044600-80045000	Enhancers	NHDF-Ad	bronchial
10	chr7:80044600-80045400	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links