Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:34306937..34309088-chr3:34310627..34313215,3	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs13061194	1.00[ASN][1000 genomes]
rs13075807	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13080986	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17280089	1.00[ASN][1000 genomes]
rs2139172	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34050472	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34272332	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34475061	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34633026	1.00[ASN][1000 genomes]
rs34811734	1.00[ASN][1000 genomes]
rs34915338	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35368076	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35489200	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4459843	1.00[ASN][1000 genomes]
rs56296977	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71325180	1.00[ASN][1000 genomes]
rs71325181	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73827388	1.00[ASN][1000 genomes]
rs7630319	1.00[ASN][1000 genomes]
rs7640851	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7652464	1.00[ASN][1000 genomes]
rs9831758	1.00[ASN][1000 genomes]
rs9852050	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
5	nsv1001752	chr3:34294343-34323331	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	1 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	chr3:34311200-34317000	Weak transcription	Thymus	Thymus
2	chr3:34311600-34312600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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