Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:14859090..14861878-chr7:14862761..14865091,3	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10085417	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10241170	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10245728	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10256424	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10257070	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10260713	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10261580	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10479935	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10487783	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1117749	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1117750	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12669279	0.88[EUR][1000 genomes]
rs17168484	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1990380	0.88[EUR][1000 genomes]
rs1990381	0.92[EUR][1000 genomes]
rs217558	0.84[EUR][1000 genomes]
rs217559	0.84[EUR][1000 genomes]
rs4719427	0.93[ASN][1000 genomes]
rs58737612	0.88[EUR][1000 genomes]
rs6461141	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7777002	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7791432	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7797480	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7802899	0.84[EUR][1000 genomes]
rs961634	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9691738	0.81[AMR][1000 genomes];0.88[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	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1020722	chr7:14792114-14871907	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14855800-14873200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:14859200-14865200	Weak transcription	Stomach Mucosa	stomach
3	chr7:14862200-14870200	Weak transcription	Osteobl	bone
4	chr7:14864000-14865000	Weak transcription	Left Ventricle	heart

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