Variant report

Variant	rs4756217
Chromosome Location	chr11:35366733-35366734
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35362046..35363846-chr11:35365711..35367318,2	MCF-7	breast:
2	chr11:35360058..35364651-chr11:35365186..35370074,5	K562	blood:
3	chr11:35366512..35368832-chr11:35383993..35385771,3	MCF-7	breast:

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];1.00[ASN][1000 genomes]
rs2421764	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3847621	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3847622	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858469	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3858470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3901811	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4755396	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4756213	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4756218	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];1.00[ASN][1000 genomes]
rs7930134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7934466	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7943314	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7945809	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35354000-35367800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:35361800-35367800	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:35361800-35368200	Weak transcription	Hela-S3	cervix
4	chr11:35362000-35368000	Weak transcription	Left Ventricle	heart
5	chr11:35362200-35366800	Weak transcription	Right Atrium	heart
6	chr11:35362200-35367800	Weak transcription	Brain Anterior Caudate	brain
7	chr11:35362400-35368400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:35362600-35372800	Weak transcription	NHLF	lung
9	chr11:35362800-35366800	Weak transcription	Pancreas	Pancrea
10	chr11:35363000-35369200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:35363200-35368600	Weak transcription	Liver	Liver
12	chr11:35363400-35367200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr11:35363400-35367200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr11:35364000-35366800	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr11:35364000-35367000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr11:35364200-35367200	Enhancers	Primary T cells fromperipheralblood	blood
17	chr11:35364600-35371600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr11:35364800-35367400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr11:35364800-35370000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr11:35365000-35367400	Enhancers	GM12878-XiMat	blood
21	chr11:35365000-35367600	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr11:35365200-35367000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr11:35365200-35367200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:35365200-35367200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:35365200-35368400	Enhancers	Primary T cells from cord blood	blood
26	chr11:35365400-35366800	Weak transcription	Fetal Thymus	thymus
27	chr11:35365400-35368000	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr11:35365600-35370400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr11:35365800-35367000	Enhancers	Brain Angular Gyrus	brain
30	chr11:35365800-35367200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:35365800-35367200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr11:35365800-35368800	Enhancers	Fetal Lung	lung
33	chr11:35365800-35369800	Enhancers	Fetal Muscle Leg	muscle
34	chr11:35366000-35366800	Enhancers	Brain Substantia Nigra	brain
35	chr11:35366000-35367200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:35366000-35367200	Enhancers	Psoas Muscle	Psoas
37	chr11:35366000-35367600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:35366000-35370400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr11:35366000-35370600	Enhancers	HepG2	liver
40	chr11:35366200-35367000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:35366200-35367000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:35366200-35367000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:35366200-35367000	Enhancers	Adipose Nuclei	Adipose
44	chr11:35366200-35367000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr11:35366200-35367200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:35366200-35367200	Enhancers	Primary B cells from peripheral blood	blood
47	chr11:35366200-35367200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr11:35366200-35367200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr11:35366200-35370800	Enhancers	Stomach Smooth Muscle	stomach
50	chr11:35366200-35371000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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