Variant report

Variant	rs11032618
Chromosome Location	chr11:34352852-34352853
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34351992..34353875-chr11:34377639..34379181,2	K562	blood:
2	chr11:34348938..34354072-chr11:34377839..34381430,6	MCF-7	breast:
3	chr11:34342106..34344369-chr11:34352747..34354682,2	MCF-7	breast:
4	chr11:34351980..34355833-chr11:34364485..34369065,5	MCF-7	breast:
5	chr11:34295048..34297358-chr11:34352691..34354542,2	MCF-7	breast:
6	chr11:34340006..34344767-chr11:34350658..34354959,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166016	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10768059	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs10768060	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs10768062	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs10768063	0.82[CHB][hapmap];0.80[CHD][hapmap];0.82[MEX][hapmap]
rs10768065	0.82[CHB][hapmap];0.81[JPT][hapmap];0.90[MEX][hapmap]
rs10768066	0.82[CHB][hapmap];0.85[TSI][hapmap]
rs10836186	0.82[CHB][hapmap];0.80[CHD][hapmap];0.81[JPT][hapmap]
rs10836190	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs11032617	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11032621	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs11032624	0.82[CHB][hapmap];0.81[JPT][hapmap];1.00[MEX][hapmap]
rs11032634	0.82[MEX][hapmap]
rs12796736	0.84[EUR][1000 genomes]
rs1883736	0.82[CHB][hapmap];0.81[JPT][hapmap];0.90[MEX][hapmap]
rs2001176	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs2145794	0.82[CHB][hapmap];0.85[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs3740795	0.82[MEX][hapmap]
rs4140544	0.82[MEX][hapmap]
rs742634	0.82[MEX][hapmap]
rs7929828	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs7944461	0.82[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757435	chr11:34220504-34370236	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759816	chr11:34220504-34370236	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv818809	chr11:34239730-34354076	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv2753052	chr11:34247462-34358300	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
7	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv818810	chr11:34337564-34354076	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
10	esv2753225	chr11:34338342-34354865	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
11	nsv897210	chr11:34349427-34381075	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a
12	nsv508622	chr11:34350559-34363184	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34336200-34358200	Weak transcription	Thymus	Thymus
2	chr11:34339000-34357400	Weak transcription	Fetal Thymus	thymus
3	chr11:34340000-34353200	Weak transcription	Small Intestine	intestine
4	chr11:34346600-34353800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:34347000-34355600	Weak transcription	GM12878-XiMat	blood
6	chr11:34347800-34354400	Enhancers	Fetal Stomach	stomach
7	chr11:34348000-34353200	Enhancers	Fetal Muscle Leg	muscle
8	chr11:34348400-34354400	Enhancers	Psoas Muscle	Psoas
9	chr11:34348600-34353600	Enhancers	Colon Smooth Muscle	Colon
10	chr11:34348600-34353800	Enhancers	Rectal Smooth Muscle	rectum
11	chr11:34349800-34353200	Enhancers	Stomach Smooth Muscle	stomach
12	chr11:34349800-34353600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:34350800-34356400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:34351000-34353000	Weak transcription	Brain Anterior Caudate	brain
15	chr11:34351000-34353800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr11:34351000-34354400	Enhancers	Aorta	Aorta
17	chr11:34351200-34353000	Weak transcription	Placenta	Placenta
18	chr11:34351200-34355000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:34351400-34353000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr11:34351400-34353200	Enhancers	Liver	Liver
21	chr11:34351600-34353000	Weak transcription	Lung	lung
22	chr11:34351600-34353000	Weak transcription	Right Ventricle	heart
23	chr11:34351600-34354400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:34351800-34354000	Enhancers	Hela-S3	cervix
25	chr11:34351800-34354400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:34351800-34363800	Weak transcription	Left Ventricle	heart
27	chr11:34352200-34353400	Enhancers	Brain Germinal Matrix	brain
28	chr11:34352200-34354000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr11:34352200-34354000	Enhancers	HSMM	muscle
30	chr11:34352200-34354000	Enhancers	Osteobl	bone
31	chr11:34352200-34354400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:34352200-34354400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:34352200-34354600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr11:34352200-34354600	Enhancers	Fetal Lung	lung
35	chr11:34352400-34353000	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr11:34352400-34353200	Enhancers	Pancreas	Pancrea
37	chr11:34352400-34353400	Enhancers	Right Atrium	heart
38	chr11:34352400-34353600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:34352400-34353800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:34352400-34353800	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr11:34352400-34354000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr11:34352400-34354000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr11:34352400-34354000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr11:34352400-34354000	Enhancers	HMEC	breast
45	chr11:34352400-34354600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr11:34352400-34354600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr11:34352400-34354800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr11:34352400-34355000	Enhancers	Brain Hippocampus Middle	brain
49	chr11:34352600-34353200	Enhancers	Brain Cingulate Gyrus	brain
50	chr11:34352600-34353600	Weak transcription	HSMMtube	muscle

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