Variant report

Variant	rs73066670
Chromosome Location	chr2:205687984-205687985
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs57445021	0.96[AFR][1000 genomes]
rs58347501	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59614427	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61099489	1.00[AMR][1000 genomes]
rs73053164	1.00[AMR][1000 genomes]
rs73054913	1.00[AMR][1000 genomes]
rs73059039	1.00[AMR][1000 genomes]
rs73059054	1.00[AMR][1000 genomes]
rs73059077	1.00[AMR][1000 genomes]
rs73060925	1.00[AMR][1000 genomes]
rs73060932	1.00[AMR][1000 genomes]
rs73066608	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066610	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066621	1.00[AMR][1000 genomes]
rs73066640	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066645	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066658	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066661	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066676	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73066678	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1010210	chr2:205489653-206076013	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2757846	chr2:205539832-205841174	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759111	chr2:205539832-205841174	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv875724	chr2:205572718-205727222	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv875725	chr2:205572718-205760800	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv875726	chr2:205588773-205700834	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv875727	chr2:205626483-205715245	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205682600-205688200	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:205686000-205692600	Weak transcription	Fetal Kidney	kidney

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