Variant report

Variant	rs17033037
Chromosome Location	chr2:67310303-67310304
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TCF7L2	chr2:67310047-67310593	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:67309863..67311895-chr2:67315048..67316901,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000235885	TF binding region
ENSG00000230906	TF binding region

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10180944	0.96[ASN][1000 genomes]
rs13404435	0.96[ASN][1000 genomes]
rs17032937	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17032952	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17032968	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17032971	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17032991	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17033005	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17033035	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17033040	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17033053	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770658	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55850737	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57035035	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58926892	0.88[ASN][1000 genomes]
rs61400784	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6546276	0.92[ASN][1000 genomes]
rs6546277	0.88[ASN][1000 genomes]
rs6546281	0.89[ASN][1000 genomes]
rs6722059	0.91[ASN][1000 genomes]
rs6751541	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890017	0.92[ASN][1000 genomes]
rs72890019	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890026	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890028	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890031	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890032	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890033	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890036	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890038	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72890041	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73937650	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7566710	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs976794	1.00[EUR][1000 genomes];0.96[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	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2756926	chr2:67266707-67337017	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2759058	chr2:67266707-67465662	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv34381	chr2:67273120-67316250	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv2757805	chr2:67287279-67465662	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv428397	chr2:67287279-67465662	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67308600-67313600	Enhancers	Colon Smooth Muscle	Colon
2	chr2:67309000-67313400	Enhancers	Fetal Lung	lung
3	chr2:67309800-67311600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr2:67310000-67313000	Enhancers	Fetal Kidney	kidney
5	chr2:67310000-67315600	Enhancers	Fetal Stomach	stomach
6	chr2:67310200-67313000	Enhancers	Rectal Smooth Muscle	rectum

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