Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:112308902..112311272-chr7:112311954..112314606,2	K562	blood:
2	chr7:112309536..112311272-chr7:112312196..112314606,2	K562	blood:
3	chr7:112288920..112291505-chr7:112309158..112311959,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10227777	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10241709	1.00[EUR][1000 genomes]
rs10258268	1.00[ASN][1000 genomes]
rs10275970	1.00[ASN][1000 genomes]
rs10277252	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12112671	1.00[EUR][1000 genomes]
rs17159980	1.00[EUR][1000 genomes]
rs2204927	1.00[ASN][1000 genomes]
rs28435304	1.00[EUR][1000 genomes]
rs28601694	1.00[EUR][1000 genomes]
rs2905281	1.00[EUR][1000 genomes]
rs2905282	1.00[EUR][1000 genomes]
rs4517054	1.00[ASN][1000 genomes]
rs56391065	1.00[ASN][1000 genomes]
rs6965803	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6968530	1.00[EUR][1000 genomes]
rs73715667	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73715670	1.00[ASN][1000 genomes]
rs73715678	1.00[ASN][1000 genomes]
rs73715679	1.00[ASN][1000 genomes]
rs73718117	1.00[EUR][1000 genomes]
rs73718119	1.00[EUR][1000 genomes]
rs7778342	1.00[EUR][1000 genomes]
rs7806160	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	nsv889055	chr7:112174089-112353440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112308000-112316200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr7:112309800-112314800	Weak transcription	HSMMtube	muscle
3	chr7:112310000-112317600	Weak transcription	Placenta	Placenta

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