Variant report

Variant	rs10096526
Chromosome Location	chr8:11567405-11567406
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11559801..11562734-chr8:11565950..11568340,2	K562	blood:

Variant related genes	Relation type
ENSG00000136574	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10088181	1.00[EUR][1000 genomes]
rs10091294	1.00[EUR][1000 genomes]
rs10094355	1.00[EUR][1000 genomes]
rs10094370	1.00[MKK][hapmap]
rs10094630	1.00[EUR][1000 genomes]
rs10096015	1.00[EUR][1000 genomes]
rs10097076	1.00[EUR][1000 genomes]
rs10100742	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10101788	1.00[EUR][1000 genomes]
rs10101900	1.00[EUR][1000 genomes]
rs10102714	1.00[EUR][1000 genomes]
rs10103483	1.00[EUR][1000 genomes]
rs10105409	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10106250	0.86[ASW][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10108287	1.00[EUR][1000 genomes]
rs10109678	1.00[EUR][1000 genomes]
rs10109971	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10111542	1.00[EUR][1000 genomes]
rs10112464	1.00[EUR][1000 genomes]
rs10113255	1.00[EUR][1000 genomes]
rs10216815	1.00[EUR][1000 genomes]
rs2127130	1.00[EUR][1000 genomes]
rs2127131	1.00[EUR][1000 genomes]
rs2244775	1.00[EUR][1000 genomes]
rs2252818	1.00[EUR][1000 genomes]
rs2252906	1.00[EUR][1000 genomes]
rs2252908	1.00[EUR][1000 genomes]
rs2252914	1.00[EUR][1000 genomes]
rs2264307	1.00[EUR][1000 genomes]
rs2409812	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs28394863	1.00[EUR][1000 genomes]
rs28472428	1.00[EUR][1000 genomes]
rs28505660	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs28665608	1.00[EUR][1000 genomes]
rs4841582	1.00[EUR][1000 genomes]
rs5027656	1.00[EUR][1000 genomes]
rs55951800	1.00[EUR][1000 genomes]
rs57782848	1.00[EUR][1000 genomes]
rs58467083	1.00[EUR][1000 genomes]
rs59035560	1.00[EUR][1000 genomes]
rs60419043	1.00[EUR][1000 genomes]
rs61265429	1.00[EUR][1000 genomes]
rs73533953	1.00[EUR][1000 genomes]
rs73545766	1.00[EUR][1000 genomes]
rs73545784	1.00[EUR][1000 genomes]
rs73663183	1.00[EUR][1000 genomes]
rs73663184	1.00[EUR][1000 genomes]
rs73663185	1.00[EUR][1000 genomes]
rs73663187	1.00[EUR][1000 genomes]
rs73663190	1.00[EUR][1000 genomes]
rs73663191	1.00[EUR][1000 genomes]
rs73663201	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7831152	1.00[EUR][1000 genomes]
rs7841968	1.00[EUR][1000 genomes]
rs8191510	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs8191543	1.00[EUR][1000 genomes]
rs8191551	0.82[MKK][hapmap]
rs8191573	1.00[EUR][1000 genomes]
rs8191664	1.00[TSI][hapmap]
rs8191669	1.00[EUR][1000 genomes]
rs8191682	1.00[TSI][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS 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	54 gene(s)	inside rSNPs	diseases
2	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv6079	chr8:11564157-11573046	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3415599	chr8:11565343-11567591	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11560400-11568400	Active TSS	Right Atrium	heart
2	chr8:11563200-11568200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr8:11564200-11568000	Active TSS	Left Ventricle	heart
4	chr8:11564200-11568600	Active TSS	Pancreas	Pancrea
5	chr8:11565000-11568200	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:11565400-11567800	Transcr. at gene 5' and 3'	Gastric	stomach
7	chr8:11565400-11568000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
8	chr8:11565400-11568200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
9	chr8:11565600-11568000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
10	chr8:11566000-11567600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr8:11566400-11568000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:11566400-11568800	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
13	chr8:11566600-11568000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:11566600-11568000	Active TSS	Right Ventricle	heart
15	chr8:11566800-11567600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
16	chr8:11566800-11567800	Bivalent/Poised TSS	Fetal Stomach	stomach
17	chr8:11567200-11567600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
18	chr8:11567200-11567600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr8:11567200-11567600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
20	chr8:11567200-11567800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr8:11567200-11567800	Flanking Active TSS	Fetal Heart	heart
22	chr8:11567200-11567800	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
23	chr8:11567200-11567800	Genic enhancers	HepG2	liver
24	chr8:11567200-11568200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr8:11567200-11574400	Enhancers	Liver	Liver
26	chr8:11567400-11567600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
27	chr8:11567400-11567800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr8:11567400-11568000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
29	chr8:11567400-11568200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:11567400-11568600	Active TSS	Duodenum Mucosa	Duodenum
31	chr8:11567400-11568600	Active TSS	Ovary	ovary

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