Variant report

Variant	rs11033078
Chromosome Location	chr11:35358401-35358402
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35358242..35359816-chr11:35412512..35414098,2	MCF-7	breast:
2	chr11:35343264..35345981-chr11:35357333..35358972,2	MCF-7	breast:
3	chr11:34930292..34932707-chr11:35355903..35358489,2	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11033085	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11033088	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12274790	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12275544	0.81[AFR][1000 genomes]
rs12279038	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12290517	0.99[ASN][1000 genomes]
rs2273686	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3847618	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3915513	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4110478	0.90[EUR][1000 genomes]
rs4996048	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59377579	0.99[ASN][1000 genomes]
rs61454047	0.99[ASN][1000 genomes]
rs7111949	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7114489	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7127728	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv832120	chr11:35277410-35490304	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh 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	11 gene(s)	inside rSNPs	diseases
3	esv2758264	chr11:35319320-35480522	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759819	chr11:35319320-35480522	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35352800-35361600	Weak transcription	Left Ventricle	heart
2	chr11:35353000-35361600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr11:35353800-35359000	Weak transcription	K562	blood
4	chr11:35354000-35359200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:35354000-35359800	Weak transcription	Pancreas	Pancrea
6	chr11:35354000-35367800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr11:35354400-35366000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr11:35354600-35358800	Weak transcription	Brain Anterior Caudate	brain
9	chr11:35354600-35359000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr11:35354600-35361600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr11:35354600-35366000	Weak transcription	Brain Substantia Nigra	brain
12	chr11:35354800-35363200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr11:35356400-35359000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:35357000-35364000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr11:35357600-35360000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:35357800-35359200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr11:35357800-35362000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:35357800-35362400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:35357800-35362800	Enhancers	NHDF-Ad	bronchial
20	chr11:35358000-35358600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr11:35358000-35358800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr11:35358000-35359000	Enhancers	Hela-S3	cervix
23	chr11:35358000-35359000	Enhancers	HMEC	breast
24	chr11:35358000-35359000	Enhancers	NHEK	skin
25	chr11:35358000-35359200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:35358000-35359400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr11:35358000-35359600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:35358000-35359600	Enhancers	Brain Hippocampus Middle	brain
29	chr11:35358000-35359600	Enhancers	HepG2	liver
30	chr11:35358000-35359800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr11:35358000-35360000	Enhancers	Osteobl	bone
32	chr11:35358000-35360800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:35358000-35361000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr11:35358000-35361000	Enhancers	NH-A	brain
35	chr11:35358000-35362600	Enhancers	NHLF	lung
36	chr11:35358200-35359400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:35358200-35359800	Enhancers	Placenta	Placenta
38	chr11:35358200-35359800	Enhancers	A549	lung
39	chr11:35358200-35360600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:35358400-35358800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:35358400-35361600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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