Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:155872011..155872725-chr3:156100054..156100965,2	K562	blood:
2	chr3:155870131..155872683-chr3:155876390..155878620,2	K562	blood:

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

rs_ID	r²[population]
rs17170	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3935399	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3936002	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4076087	0.80[ASN][1000 genomes]
rs4234309	0.80[ASN][1000 genomes]
rs4234310	0.84[EUR][1000 genomes]
rs4234311	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4472010	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4533601	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4580504	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4611771	0.89[EUR][1000 genomes]
rs4680238	0.91[ASN][1000 genomes]
rs4680239	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6441038	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6441039	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6441040	0.80[ASN][1000 genomes]
rs6784723	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7625226	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7625723	0.80[ASN][1000 genomes]
rs7627867	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9832745	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv592085	chr3:155827634-156012679	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr3:155868600-155873200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr3:155870200-155874200	Weak transcription	Left Ventricle	heart
3	chr3:155870200-155875800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:155870200-155876400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:155870400-155917800	Weak transcription	Aorta	Aorta

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