Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:113583124..113585707-chr5:113637136..113639363,2	K562	blood:

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10038304	0.82[EUR][1000 genomes]
rs10041267	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10043950	0.81[EUR][1000 genomes]
rs10045558	0.82[EUR][1000 genomes]
rs10463657	0.84[EUR][1000 genomes]
rs10900693	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11241267	0.82[EUR][1000 genomes]
rs12153188	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12523408	0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12652393	0.82[EUR][1000 genomes]
rs4074169	0.87[EUR][1000 genomes]
rs4131322	0.84[EUR][1000 genomes]
rs4293905	0.81[ASN][1000 genomes]
rs4429843	0.82[EUR][1000 genomes]
rs4482897	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4485916	0.85[ASN][1000 genomes]
rs4505938	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4615290	0.82[EUR][1000 genomes]
rs61415455	0.81[EUR][1000 genomes]
rs6594788	0.81[EUR][1000 genomes]
rs6594797	0.84[EUR][1000 genomes]
rs6594801	0.89[EUR][1000 genomes]
rs6859418	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6862991	0.81[EUR][1000 genomes]
rs6872938	0.87[EUR][1000 genomes]
rs6891422	0.84[EUR][1000 genomes]
rs6894277	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7701720	0.82[EUR][1000 genomes]
rs9326913	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882727	chr5:113548400-113602162	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1029021	chr5:113551892-113599644	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv537865	chr5:113551892-113599644	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113579400-113585600	Weak transcription	Fetal Heart	heart
2	chr5:113581400-113585800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:113581600-113586000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:113584600-113586600	Enhancers	Fetal Stomach	stomach
5	chr5:113584600-113587200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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