Variant report

Variant	rs34342012
Chromosome Location	chr7:84912193-84912194
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12534830	0.96[ASN][1000 genomes]
rs1429748	0.90[ASN][1000 genomes]
rs1527928	0.99[ASN][1000 genomes]
rs1527929	0.99[ASN][1000 genomes]
rs17159741	0.81[AFR][1000 genomes]
rs1918708	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1918709	0.99[ASN][1000 genomes]
rs2033294	0.90[ASN][1000 genomes]
rs2564780	0.90[ASN][1000 genomes]
rs2696163	0.85[ASN][1000 genomes]
rs2696164	0.99[ASN][1000 genomes]
rs2696169	0.85[ASN][1000 genomes]
rs2696173	0.95[ASN][1000 genomes]
rs2732719	0.99[ASN][1000 genomes]
rs2732720	0.99[ASN][1000 genomes]
rs2732721	0.99[ASN][1000 genomes]
rs2732722	0.99[ASN][1000 genomes]
rs2732726	0.85[ASN][1000 genomes]
rs2732731	0.84[ASN][1000 genomes]
rs2732768	0.91[ASN][1000 genomes]
rs2732770	0.99[ASN][1000 genomes]
rs2888404	0.86[ASN][1000 genomes]
rs4275151	0.93[ASN][1000 genomes]
rs4333515	0.95[ASN][1000 genomes]
rs715223	0.84[ASN][1000 genomes]
rs7804395	0.85[ASN][1000 genomes]
rs953072	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422324	chr7:84530290-84944913	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
2	nsv916645	chr7:84678606-85420011	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv869255	chr7:84678606-85444155	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1017834	chr7:84832489-85083958	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv538996	chr7:84832489-85083958	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv888647	chr7:84866308-85091003	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3327487	chr7:84901505-85320690	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr7:84906200-84916000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:84912000-84916000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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