Variant report

Variant	rs182520394
Chromosome Location	chr4:69138967-69138968
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008084	chr4:68797598-69482831	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv537131	chr4:68797598-69482831	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv1812438	chr4:68943858-69154222	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv1806586	chr4:68943858-69592846	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv461546	chr4:69049643-69223057	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv594506	chr4:69049643-69223057	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv964740	chr4:69137797-69159003	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69137800-69139000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr4:69137800-69139000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:69137800-69139200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr4:69138000-69139800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:69138000-69140400	Enhancers	Fetal Intestine Small	intestine
6	chr4:69138200-69139000	Enhancers	NHEK	skin
7	chr4:69138200-69139400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:69138200-69139400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr4:69138200-69139400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:69138200-69139400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:69138200-69139600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:69138200-69139600	Enhancers	HSMM	muscle
13	chr4:69138200-69140400	Enhancers	Fetal Intestine Large	intestine
14	chr4:69138400-69139000	Enhancers	Fetal Kidney	kidney
15	chr4:69138400-69139000	Enhancers	NHDF-Ad	bronchial
16	chr4:69138400-69139400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:69138400-69139400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:69138400-69139400	Enhancers	NH-A	brain
19	chr4:69138400-69139600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:69138400-69139600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr4:69138400-69139600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:69138400-69140800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:69138600-69139000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:69138600-69139000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:69138600-69139000	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr4:69138600-69139200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr4:69138600-69139800	Enhancers	Osteobl	bone
28	chr4:69138600-69140400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:69138800-69139000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:69138800-69139200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:69138800-69139400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr4:69138800-69139400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr4:69138800-69140000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:69138800-69140000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:69138800-69143600	Weak transcription	Muscle Satellite Cultured Cells	--

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