Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12630202	1.00[CHB][hapmap]
rs13061194	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13067818	1.00[ASN][1000 genomes]
rs13075807	1.00[ASN][1000 genomes]
rs13080986	1.00[ASN][1000 genomes]
rs2053425	1.00[CHB][hapmap]
rs2139172	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34050472	1.00[ASN][1000 genomes]
rs34272332	1.00[ASN][1000 genomes]
rs34475061	1.00[ASN][1000 genomes]
rs34633026	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34811734	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34915338	1.00[ASN][1000 genomes]
rs35489200	1.00[ASN][1000 genomes]
rs4459843	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56296977	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71325180	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71325181	1.00[ASN][1000 genomes]
rs73827388	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7630319	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7640851	1.00[ASN][1000 genomes]
rs7652464	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9831758	0.92[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9852050	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001599	chr3:34149575-34437701	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv536533	chr3:34149575-34437701	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv876682	chr3:34149814-34401451	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv916961	chr3:34203879-34506554	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34280200-34283200	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr3:34281600-34283800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:34281800-34282200	Enhancers	Fetal Intestine Large	intestine
4	chr3:34281800-34282600	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr3:34281800-34282800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:34281800-34283000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr3:34281800-34283200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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