Variant report

Variant	rs11038860
Chromosome Location	chr11:46339184-46339185
allele	C/T
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46332850..46336824-chr11:46338704..46341793,4	MCF-7	breast:
2	chr11:46296655..46299428-chr11:46337321..46339943,2	K562	blood:
3	chr11:46259014..46262894-chr11:46335326..46342667,9	K562	blood:
4	chr11:46337829..46340828-chr11:46350846..46352453,2	K562	blood:
5	chr11:46337540..46339724-chr11:46341786..46344152,2	K562	blood:
6	chr11:46332816..46336115-chr11:46338065..46341481,4	K562	blood:
7	chr11:46336628..46338885-chr11:46339092..46341435,2	K562	blood:
8	chr11:46257955..46261525-chr11:46335370..46339844,7	K562	blood:
9	chr11:46338683..46341557-chr11:46343415..46346648,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000157613	Chromatin interaction
ENSG00000254639	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10838596	0.84[ASW][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7476	0.84[ASW][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv554201	chr11:46281835-46422686	Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv825867	chr11:46303184-46425613	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv1797501	chr11:46315437-46402521	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	esv1811345	chr11:46317062-46438072	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv554202	chr11:46334239-46469900	Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46319200-46342000	Weak transcription	Ovary	ovary
2	chr11:46319400-46346000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:46321400-46340200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:46322000-46345000	Weak transcription	Small Intestine	intestine
5	chr11:46329000-46344000	Strong transcription	Fetal Intestine Large	intestine
6	chr11:46329200-46346800	Weak transcription	Fetal Kidney	kidney
7	chr11:46330000-46341800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:46330200-46349400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr11:46330600-46339800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr11:46330600-46339800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:46330600-46344800	Strong transcription	Fetal Intestine Small	intestine
12	chr11:46330600-46345000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:46330600-46346200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr11:46330600-46348200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr11:46330600-46348800	Strong transcription	Fetal Stomach	stomach
16	chr11:46330800-46340600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr11:46330800-46344600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr11:46330800-46348200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr11:46331200-46344200	Strong transcription	Osteobl	bone
20	chr11:46331400-46344800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:46331400-46345000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:46331600-46339200	Weak transcription	Primary B cells from cord blood	blood
23	chr11:46331600-46343800	Strong transcription	NHLF	lung
24	chr11:46331600-46345000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:46331800-46339800	Weak transcription	GM12878-XiMat	blood
26	chr11:46331800-46344000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr11:46332000-46344600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:46332200-46344200	Strong transcription	Placenta Amnion	Placenta Amnion
29	chr11:46333200-46340800	Strong transcription	Fetal Lung	lung
30	chr11:46334400-46340000	Weak transcription	Lung	lung
31	chr11:46334400-46346000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr11:46335800-46345000	Strong transcription	NH-A	brain
33	chr11:46336400-46340400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr11:46336400-46341800	Enhancers	Primary hematopoietic stem cells	blood
35	chr11:46336400-46345200	Strong transcription	HSMM	muscle
36	chr11:46336600-46339800	Strong transcription	Fetal Muscle Leg	muscle
37	chr11:46336600-46339800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr11:46336600-46340000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:46336600-46344000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:46336600-46344800	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr11:46336800-46340400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:46336800-46343000	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr11:46336800-46346800	Weak transcription	Colon Smooth Muscle	Colon
44	chr11:46337000-46339600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr11:46337000-46339800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr11:46337000-46340000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:46337000-46340200	Weak transcription	Dnd41	blood
48	chr11:46337000-46340600	Weak transcription	Brain Hippocampus Middle	brain
49	chr11:46337000-46341400	Enhancers	Spleen	Spleen
50	chr11:46337000-46343800	Strong transcription	Rectal Mucosa Donor 31	rectum

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