Variant report

Variant	rs201130148
Chromosome Location	chr11:65688825-65688826
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:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65686637..65688948-chr11:65818033..65819758,2	MCF-7	breast:
2	chr11:65683165..65691632-chr11:65723620..65730701,28	MCF-7	breast:
3	chr11:65686026..65690385-chr11:65711034..65716101,7	MCF-7	breast:
4	chr11:65624095..65629782-chr11:65682347..65689302,13	MCF-7	breast:
5	chr11:65556129..65558020-chr11:65687401..65689807,2	MCF-7	breast:
6	chr11:65650579..65663306-chr11:65677153..65690311,39	MCF-7	breast:
7	chr11:65622510..65630779-chr11:65675126..65689187,23	MCF-7	breast:
8	chr11:65478095..65481080-chr11:65686637..65690416,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRAP1-1	chr11:65688523-65688996	NONHSAT022244

No data

Variant related genes	Relation type
ENSG00000172818	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000175513	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000175602	Chromatin interaction
ENSG00000255120	Chromatin interaction
ENSG00000087365	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000172500	Chromatin interaction
ENSG00000172977	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
2	esv2758274	chr11:65559893-65722363	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
3	esv2759834	chr11:65559893-65722363	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv427890	chr11:65559893-65722363	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
5	nsv897761	chr11:65580638-65738566	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	186 gene(s)	inside rSNPs	diseases
6	nsv897762	chr11:65613218-65758854	Active TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	185 gene(s)	inside rSNPs	diseases
7	nsv897764	chr11:65613348-65695222	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
8	nsv897765	chr11:65623708-65758854	Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
9	nsv832191	chr11:65632329-65806120	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
10	nsv897767	chr11:65683531-65690206	Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
11	esv3444925	chr11:65687425-65714023	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
12	nsv972039	chr11:65688555-65692860	Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65687200-65689000	Enhancers	Fetal Brain Male	brain
2	chr11:65687600-65690800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:65687600-65691000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:65687800-65689000	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:65687800-65689000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:65687800-65699800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:65688000-65689400	Weak transcription	Aorta	Aorta
8	chr11:65688000-65689800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr11:65688000-65690600	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
10	chr11:65688000-65691200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:65688000-65692400	Weak transcription	Fetal Kidney	kidney
12	chr11:65688200-65689000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:65688200-65689000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr11:65688200-65689000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr11:65688200-65689000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:65688200-65689000	Transcr. at gene 5' and 3'	HMEC	breast
17	chr11:65688200-65689400	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:65688200-65689600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:65688200-65689800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr11:65688200-65690000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:65688200-65690000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr11:65688200-65691000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:65688200-65691200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:65688200-65695200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:65688400-65689000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:65688400-65689000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:65688400-65689000	Enhancers	Pancreas	Pancrea
28	chr11:65688400-65689600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr11:65688400-65689600	Weak transcription	Left Ventricle	heart
30	chr11:65688400-65689800	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:65688400-65690600	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:65688400-65694600	Weak transcription	K562	blood
33	chr11:65688600-65689000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:65688600-65689000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr11:65688600-65689000	Genic enhancers	Brain Germinal Matrix	brain
36	chr11:65688600-65689000	Genic enhancers	Dnd41	blood
37	chr11:65688600-65689200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr11:65688600-65689200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
39	chr11:65688600-65689200	Weak transcription	Brain Angular Gyrus	brain
40	chr11:65688600-65689200	Weak transcription	Gastric	stomach
41	chr11:65688600-65689200	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr11:65688600-65689400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:65688600-65689400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr11:65688600-65689400	Weak transcription	Colonic Mucosa	Colon
45	chr11:65688600-65689400	Weak transcription	Esophagus	oesophagus
46	chr11:65688600-65689400	Weak transcription	Ovary	ovary
47	chr11:65688600-65689400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr11:65688600-65689400	Weak transcription	GM12878-XiMat	blood
49	chr11:65688600-65689400	Weak transcription	HSMMtube	muscle
50	chr11:65688600-65689400	Weak transcription	NHEK	skin

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