Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:14503536..14506450-chr7:14511181..14513157,3	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10950525	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10950526	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10950529	0.93[EUR][1000 genomes]
rs12531006	0.94[ASN][1000 genomes]
rs12532388	0.94[ASN][1000 genomes]
rs12533729	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12533779	0.84[EUR][1000 genomes]
rs12538874	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12540039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12540646	0.94[ASN][1000 genomes]
rs12673303	0.88[EUR][1000 genomes]
rs12674246	0.88[EUR][1000 genomes]
rs1431523	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16878172	0.95[EUR][1000 genomes]
rs16878192	0.81[EUR][1000 genomes]
rs2060160	0.88[EUR][1000 genomes]
rs59470727	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs59778011	0.94[ASN][1000 genomes]
rs61207348	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61487234	0.84[EUR][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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14504800-14505800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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