Variant report

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	USF2	chr11:101979274-101979406	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr11:101979285-101979497	MCF10A-Er-Src	breast:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:101923063..101925584-chr11:101978678..101981062,2	MCF-7	breast:
2	chr11:66823134..66824640-chr11:101978587..101981113,2	MCF-7	breast:
3	chr11:101973697..101975768-chr11:101978687..101980575,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YAP1-1	chr11:101978617-101980573	ENSG00000260008.1

No data

Variant related genes	Relation type
YAP1	TF binding region
ENSG00000173156	Chromatin interaction

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

rs_ID	r²[population]
rs12417039	0.85[ASN][1000 genomes]
rs12417236	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12420608	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17097445	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1942681	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4754039	0.85[ASN][1000 genomes]
rs4754040	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4754832	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57102842	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58421489	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58715614	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73577816	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73577857	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73577867	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73577889	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73577900	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73579981	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73582014	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs948736	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs974830	0.93[AMR][1000 genomes];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	esv3362945	chr11:101736547-102114246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898333	chr11:101832670-102079986	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101968000-101980400	Weak transcription	Right Atrium	heart
2	chr11:101976400-101979800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:101978200-101979400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:101978600-101980200	Enhancers	HepG2	liver
5	chr11:101979200-101979400	Enhancers	Esophagus	oesophagus
6	chr11:101979200-101980000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:101979200-101980000	Enhancers	Hela-S3	cervix
8	chr11:101979200-101980200	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr11:101979200-101980200	Enhancers	NHDF-Ad	bronchial

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