Variant report

Variant	rs55653360
Chromosome Location	chr11:64102321-64102322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64067284..64069866-chr11:64101359..64103336,2	MCF-7	breast:
2	chr11:64099746..64102577-chr11:64121757..64123741,2	K562	blood:
3	chr11:64097645..64100865-chr11:64101163..64102730,3	K562	blood:
4	chr11:64101319..64104244-chr11:64105881..64108198,2	MCF-7	breast:
5	chr11:64101193..64104883-chr11:64108788..64111496,4	MCF-7	breast:
6	chr11:63973100..63975827-chr11:64099770..64102904,4	K562	blood:
7	chr11:64102252..64103199-chr11:64122319..64123180,2	K562	blood:
8	chr11:64097984..64104274-chr11:64108545..64113861,10	MCF-7	breast:
9	chr11:64005747..64008730-chr11:64101286..64103643,2	K562	blood:
10	chr11:64096689..64098534-chr11:64100338..64102501,2	MCF-7	breast:
11	chr11:64033644..64035554-chr11:64101118..64102657,2	K562	blood:
12	chr11:64035765..64039535-chr11:64101198..64104019,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000173486	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000236935	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs41294390	1.00[ASN][1000 genomes]
rs45553131	1.00[ASN][1000 genomes]
rs45615733	1.00[AMR][1000 genomes]
rs55697310	1.00[AMR][1000 genomes]
rs56268570	1.00[AMR][1000 genomes]
rs57437106	1.00[AMR][1000 genomes]
rs58127892	1.00[AMR][1000 genomes]
rs58851354	1.00[AMR][1000 genomes]
rs59413043	1.00[AMR][1000 genomes]
rs60080768	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61578679	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
6	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
7	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
8	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
10	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
11	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
12	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
13	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
14	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
15	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
16	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
17	nsv555192	chr11:64097233-64111928	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	n/a
18	nsv818840	chr11:64097233-64125142	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer 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 miRNA	33 gene(s)	inside rSNPs	diseases
19	nsv818841	chr11:64097233-64129722	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64087000-64108200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:64089400-64106800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr11:64091600-64106400	Weak transcription	Primary T cells from cord blood	blood
4	chr11:64099400-64102400	Weak transcription	HSMMtube	muscle
5	chr11:64099400-64102600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:64099600-64102400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:64099600-64102600	Weak transcription	Fetal Heart	heart
8	chr11:64099600-64102600	Weak transcription	Right Atrium	heart
9	chr11:64099600-64107600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:64099800-64102600	Weak transcription	Gastric	stomach
11	chr11:64099800-64102600	Weak transcription	Right Ventricle	heart
12	chr11:64099800-64105600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr11:64099800-64106400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr11:64099800-64106400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr11:64099800-64106400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr11:64099800-64106400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr11:64099800-64106800	Weak transcription	Thymus	Thymus
18	chr11:64099800-64107600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr11:64099800-64108000	Weak transcription	Brain Anterior Caudate	brain
20	chr11:64099800-64108000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr11:64099800-64108200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr11:64099800-64108400	Weak transcription	Left Ventricle	heart
23	chr11:64099800-64109600	Weak transcription	Liver	Liver
24	chr11:64100000-64102400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr11:64100000-64102400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:64100000-64102400	Weak transcription	HSMM	muscle
27	chr11:64100000-64102400	Weak transcription	NHDF-Ad	bronchial
28	chr11:64100000-64102400	Weak transcription	Osteobl	bone
29	chr11:64100000-64102600	Weak transcription	HUVEC	blood vessel
30	chr11:64100000-64104800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:64100000-64104800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:64100000-64105000	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr11:64100000-64105600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:64100000-64106400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr11:64100000-64106400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr11:64100000-64106600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr11:64100000-64107000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr11:64100000-64109000	Weak transcription	Pancreas	Pancrea
39	chr11:64100200-64102400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:64100200-64102400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr11:64100200-64102400	Weak transcription	Spleen	Spleen
42	chr11:64100200-64102400	Enhancers	Hela-S3	cervix
43	chr11:64100200-64102400	Weak transcription	NH-A	brain
44	chr11:64100200-64102600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:64100200-64102600	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr11:64100200-64106400	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr11:64100200-64107000	Weak transcription	Esophagus	oesophagus
48	chr11:64100200-64108000	Weak transcription	Lung	lung
49	chr11:64100200-64108200	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr11:64100400-64102400	Weak transcription	Primary hematopoietic stem cells	blood

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