Variant report

No.	Distal block	Cell Line	Cell type
1	chr19:39694662..39698816-chr19:39700094..39703085,3	K562	blood:
2	chr19:39702433..39703702-chr19:39818478..39819662,6	MCF-7	breast:
3	chr19:39612566..39613389-chr19:39702383..39703279,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000179751	Chromatin interaction

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11083512	0.82[CHB][hapmap]
rs11083514	0.83[CHB][hapmap]
rs11083515	0.83[CHB][hapmap]
rs11083516	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11083517	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11672787	0.83[CHB][hapmap]
rs11882959	0.83[CHB][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs11883201	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11883239	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12462614	0.87[CHB][hapmap]
rs12463249	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12610064	0.87[CHB][hapmap]
rs12610093	0.87[CHB][hapmap]
rs12610618	0.83[CHB][hapmap]
rs12975799	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12981390	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2319156	0.87[CHB][hapmap]
rs35408086	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7245516	0.95[ASN][1000 genomes]
rs8100659	0.83[CHB][hapmap]
rs8104935	0.83[CHB][hapmap]
rs8106521	0.87[CHB][hapmap]
rs8107090	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs892015	0.87[CHB][hapmap]
rs892016	0.87[CHB][hapmap]

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	nsv833829	chr19:39569681-39730777	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv432048	chr19:39572060-39850060	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv1796470	chr19:39679379-39714631	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv518540	chr19:39697974-39731783	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region 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	chr19:39699200-39705600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr19:39702200-39703200	Enhancers	A549	lung
3	chr19:39702800-39703200	Enhancers	Esophagus	oesophagus

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