Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:98791055-98791244	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:98783900..98786083-chr9:98790874..98793453,2	K562	blood:
2	chr9:98790248..98792722-chr9:98793401..98795775,2	MCF-7	breast:
3	chr9:98790389..98794152-chr9:98794649..98798124,5	K562	blood:

Variant related genes	Relation type
LINC00092	TF binding region
ENSG00000225194	Chromatin interaction

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10481697	1.00[EUR][1000 genomes]
rs10481698	1.00[EUR][1000 genomes]
rs11999390	1.00[EUR][1000 genomes]
rs12340544	1.00[EUR][1000 genomes]
rs55989349	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58506259	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73536566	1.00[EUR][1000 genomes]
rs73536567	1.00[EUR][1000 genomes]
rs73536571	1.00[EUR][1000 genomes]
rs73536572	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73654815	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73654817	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73654819	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73654820	1.00[EUR][1000 genomes]
rs73654822	1.00[EUR][1000 genomes]
rs73654824	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893599	chr9:98542410-98991254	Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
2	nsv524266	chr9:98780606-98804274	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3354669	chr9:98786831-98791329	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98789800-98793200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr9:98790000-98793600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr9:98790200-98792600	Weak transcription	Gastric	stomach
4	chr9:98790200-98793000	Weak transcription	Lung	lung
5	chr9:98790200-98793000	Weak transcription	Pancreas	Pancrea
6	chr9:98790200-98793200	Weak transcription	Brain Hippocampus Middle	brain
7	chr9:98790200-98793200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr9:98790200-98793400	Weak transcription	Right Ventricle	heart
9	chr9:98790200-98795800	Weak transcription	Esophagus	oesophagus
10	chr9:98790400-98792000	Weak transcription	Ovary	ovary
11	chr9:98790400-98792200	Weak transcription	Liver	Liver
12	chr9:98790400-98793000	Weak transcription	Right Atrium	heart
13	chr9:98790400-98793800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr9:98790400-98794200	Weak transcription	Spleen	Spleen
15	chr9:98790600-98793200	Weak transcription	Brain Anterior Caudate	brain
16	chr9:98790800-98792000	Weak transcription	Aorta	Aorta
17	chr9:98790800-98793400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr9:98790800-98810800	Weak transcription	Brain Angular Gyrus	brain
19	chr9:98791000-98793000	Weak transcription	Fetal Lung	lung
20	chr9:98791200-98793200	Weak transcription	Brain Substantia Nigra	brain
21	chr9:98791200-98796800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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