Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:103562037..103563757-chr7:103575522..103577344,2	K562	blood:
2	chr7:103532058..103533775-chr7:103563141..103565632,2	K562	blood:
3	chr7:103561421..103564064-chr7:103629667..103633796,3	K562	blood:

Variant related genes	Relation type
ENSG00000189056	Chromatin interaction

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

rs_ID	r²[population]
rs10277802	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10487175	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12154742	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs16872993	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16873008	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2192305	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs55833200	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57179739	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58352612	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58751603	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59086068	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73712299	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73712302	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73715903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73715905	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73715906	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73715908	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73715910	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73715920	0.81[ASN][1000 genomes]
rs756435	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv523466	chr7:103547135-103567525	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv933391	chr7:103557392-103588539	Weak transcription Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv971218	chr7:103561948-103585213	Weak transcription Enhancers Strong transcription	Chromatin interactive region	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	chr7:103556800-103574400	Weak transcription	HepG2	liver
2	chr7:103561600-103564400	Enhancers	K562	blood

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