Variant report

Variant	rs10836265
Chromosome Location	chr11:34637669-34637670
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34622016..34626475-chr11:34634436..34638216,4	K562	blood:
2	chr11:34630414..34634068-chr11:34634518..34638275,4	K562	blood:
3	chr11:34635743..34637873-chr11:34640545..34642777,2	MCF-7	breast:
4	chr11:34636591..34639516-chr11:34641678..34643753,2	K562	blood:
5	chr11:34636228..34637747-chr11:34653006..34655349,2	K562	blood:

Variant related genes	Relation type
ENSG00000135373	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10768085	0.80[TSI][hapmap]
rs11032786	0.83[ASN][1000 genomes]
rs1466209	0.83[EUR][1000 genomes]
rs16925915	0.90[CHD][hapmap]
rs2123650	0.96[AFR][1000 genomes]
rs717582	0.84[CHD][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs7945550	0.87[TSI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832116	chr11:34539536-34673900	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr11:34608400-34643600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:34625400-34642800	Weak transcription	Gastric	stomach
3	chr11:34628400-34638600	Weak transcription	Small Intestine	intestine
4	chr11:34628600-34637800	Weak transcription	Stomach Mucosa	stomach
5	chr11:34634000-34643200	Weak transcription	Lung	lung
6	chr11:34635000-34643400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr11:34635200-34638600	Weak transcription	Pancreas	Pancrea
8	chr11:34635200-34642000	Weak transcription	Esophagus	oesophagus
9	chr11:34636200-34638600	Weak transcription	Right Atrium	heart
10	chr11:34636200-34639600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:34636200-34641000	Weak transcription	Fetal Intestine Small	intestine
12	chr11:34636200-34644000	Enhancers	K562	blood
13	chr11:34636400-34637800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr11:34636400-34641800	Weak transcription	Fetal Intestine Large	intestine
15	chr11:34636600-34638400	Enhancers	Fetal Heart	heart
16	chr11:34636600-34640800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:34636600-34641400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:34636800-34638400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:34636800-34640800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:34637200-34637800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr11:34637200-34638000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr11:34637200-34638000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:34637200-34641600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr11:34637400-34637800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr11:34637400-34637800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr11:34637400-34641000	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr11:34637400-34641200	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr11:34637600-34637800	Enhancers	Adipose Nuclei	Adipose
29	chr11:34637600-34638000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr11:34637600-34639800	Enhancers	Right Ventricle	heart
31	chr11:34637600-34640400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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