Variant report

Variant	rs4756218
Chromosome Location	chr11:35370113-35370114
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35367767..35370379-chr11:35370546..35372523,3	K562	blood:
2	chr11:35369719..35371293-chr11:35371754..35374136,2	MCF-7	breast:
3	chr11:35360349..35364651-chr11:35366832..35371612,5	K562	blood:

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

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

rs_ID	r²[population]
rs10836375	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11033084	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2421764	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3847621	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3847622	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3858469	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3858470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3901811	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4755396	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756213	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4756217	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6484784	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7930134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7934466	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7943314	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7945809	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[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:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35362600-35372800	Weak transcription	NHLF	lung
2	chr11:35364600-35371600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:35365600-35370400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr11:35366000-35370400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr11:35366000-35370600	Enhancers	HepG2	liver
6	chr11:35366200-35370800	Enhancers	Stomach Smooth Muscle	stomach
7	chr11:35366200-35371000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:35366200-35372000	Weak transcription	K562	blood
9	chr11:35366800-35371600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr11:35367000-35370200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:35367000-35385400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr11:35367200-35370600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr11:35367200-35370600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:35367200-35370800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr11:35367200-35371200	Weak transcription	Fetal Thymus	thymus
16	chr11:35367200-35374000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr11:35367200-35374000	Weak transcription	Gastric	stomach
18	chr11:35367200-35380200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:35367600-35371600	Enhancers	NHDF-Ad	bronchial
20	chr11:35367800-35370200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:35367800-35370800	Enhancers	Placenta	Placenta
22	chr11:35368000-35370200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:35368000-35372400	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr11:35368400-35370200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:35368400-35371600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr11:35368400-35374000	Weak transcription	Left Ventricle	heart
27	chr11:35368600-35371000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr11:35368600-35371000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:35368600-35379800	Weak transcription	Brain Anterior Caudate	brain
30	chr11:35369000-35370200	Weak transcription	Primary T cells from cord blood	blood
31	chr11:35369000-35370200	Enhancers	Aorta	Aorta
32	chr11:35369000-35370200	Enhancers	HMEC	breast
33	chr11:35369000-35373800	Weak transcription	Right Atrium	heart
34	chr11:35369200-35370200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr11:35369400-35371200	Weak transcription	Hela-S3	cervix
36	chr11:35369400-35371600	Enhancers	Primary T cells fromperipheralblood	blood
37	chr11:35369400-35373800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:35369600-35370800	Enhancers	Pancreas	Pancrea
39	chr11:35369600-35372000	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr11:35369600-35372200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr11:35369600-35372400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr11:35369600-35372800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:35369800-35370600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr11:35369800-35370800	Weak transcription	Brain Hippocampus Middle	brain
45	chr11:35369800-35371800	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr11:35369800-35372800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr11:35369800-35373400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:35369800-35374000	Weak transcription	Fetal Muscle Leg	muscle
49	chr11:35369800-35374200	Weak transcription	Liver	Liver
50	chr11:35370000-35370200	Enhancers	HSMMtube	muscle

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