Variant report

Variant	rs10766366
Chromosome Location	chr11:17003071-17003072
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:16996626..17000145-chr11:17001852..17005291,4	K562	blood:
2	chr11:17003043..17005299-chr11:17227966..17230584,3	MCF-7	breast:
3	chr11:16997842..17006545-chr11:17033236..17037894,15	MCF-7	breast:
4	chr11:16976871..16981000-chr11:17000472..17004649,3	MCF-7	breast:
5	chr11:16999245..17001608-chr11:17002120..17006650,5	MCF-7	breast:
6	chr11:17002569..17005587-chr11:17010572..17013703,3	K562	blood:
7	chr11:17001912..17011357-chr11:17032509..17037700,15	MCF-7	breast:

Variant related genes	Relation type
ENSG00000070081	Chromatin interaction
ENSG00000184669	Chromatin interaction
ENSG00000166689	Chromatin interaction
ENSG00000011405	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10734250	0.80[AFR][1000 genomes]
rs10766367	0.90[EUR][1000 genomes]
rs10832707	0.92[EUR][1000 genomes]
rs10832709	0.90[EUR][1000 genomes]
rs10832710	0.88[EUR][1000 genomes]
rs10832712	0.90[EUR][1000 genomes]
rs11529141	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2302207	0.90[EUR][1000 genomes]
rs2353369	0.92[EUR][1000 genomes]
rs4237715	0.92[EUR][1000 genomes]
rs4237716	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4469869	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4757468	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757470	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757472	0.91[EUR][1000 genomes]
rs4757473	0.86[AFR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4757474	0.90[EUR][1000 genomes]
rs4757475	0.90[EUR][1000 genomes]
rs4757476	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4757483	0.80[AFR][1000 genomes]
rs6486333	0.91[EUR][1000 genomes]
rs6486334	0.90[EUR][1000 genomes]
rs7118307	0.92[EUR][1000 genomes]
rs7122802	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7934567	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7944490	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][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	nsv832077	chr11:16834545-17059176	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	esv3328361	chr11:17002851-17003177	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16982200-17003800	Weak transcription	Right Ventricle	heart
2	chr11:16992200-17007400	Weak transcription	Colonic Mucosa	Colon
3	chr11:16997600-17003200	Enhancers	Brain Anterior Caudate	brain
4	chr11:16997600-17004600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:16998000-17005000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:16998000-17009000	Enhancers	Stomach Mucosa	stomach
7	chr11:16998000-17011800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:16998200-17003200	Weak transcription	Aorta	Aorta
9	chr11:16998600-17004200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:16998800-17007800	Genic enhancers	Fetal Intestine Small	intestine
11	chr11:17000600-17004600	Enhancers	Fetal Intestine Large	intestine
12	chr11:17000600-17011800	Enhancers	Pancreas	Pancrea
13	chr11:17000800-17006200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:17001200-17003400	Enhancers	Brain Hippocampus Middle	brain
15	chr11:17001200-17003600	Enhancers	Brain Cingulate Gyrus	brain
16	chr11:17001200-17004600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:17001200-17004800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:17001400-17004200	Enhancers	Fetal Muscle Trunk	muscle
19	chr11:17001400-17004800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:17001400-17005000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:17001400-17005200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:17001400-17005200	Enhancers	Brain Angular Gyrus	brain
23	chr11:17001400-17005400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:17001400-17010600	Enhancers	Placenta	Placenta
25	chr11:17001600-17004000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr11:17001600-17005200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr11:17001800-17003800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr11:17001800-17004000	Enhancers	NH-A	brain
29	chr11:17001800-17006600	Weak transcription	Liver	Liver
30	chr11:17002000-17003200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr11:17002000-17004800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr11:17002000-17006000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr11:17002200-17003200	Weak transcription	Gastric	stomach
34	chr11:17002200-17003200	Weak transcription	Lung	lung
35	chr11:17002200-17003200	Weak transcription	A549	lung
36	chr11:17002400-17003200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:17002400-17004400	Enhancers	HMEC	breast
38	chr11:17002600-17003600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr11:17002600-17003800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr11:17002600-17004000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr11:17002600-17004200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr11:17002600-17004200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:17002600-17004800	Enhancers	Fetal Muscle Leg	muscle
44	chr11:17002600-17005000	Enhancers	Fetal Kidney	kidney
45	chr11:17002800-17003400	Enhancers	Esophagus	oesophagus
46	chr11:17002800-17003400	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr11:17002800-17003800	Enhancers	Fetal Brain Male	brain
48	chr11:17002800-17004000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr11:17002800-17004000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr11:17002800-17004000	Enhancers	Placenta Amnion	Placenta Amnion

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