Variant report

Variant	rs376084775
Chromosome Location	chr14:38889095-38889096
allele	A/C
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	nsv533235	chr14:38558180-39117391	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv530640	chr14:38702117-38927901	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2754119	chr14:38825349-38988849	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv1846932	chr14:38842788-38944821	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv510632	chr14:38868313-38939927	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv564409	chr14:38870456-38930054	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv901655	chr14:38887881-39019800	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38888000-38890000	Enhancers	Brain Germinal Matrix	brain
2	chr14:38888800-38889200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:38888800-38889200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:38888800-38889200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr14:38888800-38889200	Enhancers	Brain Cingulate Gyrus	brain
6	chr14:38888800-38889200	Active TSS	Brain Hippocampus Middle	brain
7	chr14:38888800-38889200	Active TSS	Fetal Brain Female	brain
8	chr14:38888800-38889200	Enhancers	Fetal Lung	lung
9	chr14:38888800-38889200	Enhancers	HepG2	liver
10	chr14:38888800-38889400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:38888800-38889400	Enhancers	HUVEC	blood vessel
12	chr14:38888800-38890000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr14:38888800-38890200	Enhancers	NHDF-Ad	bronchial
14	chr14:38888800-38890400	Enhancers	NHLF	lung
15	chr14:38889000-38889200	Enhancers	Aorta	Aorta
16	chr14:38889000-38889200	Flanking Active TSS	Brain Anterior Caudate	brain
17	chr14:38889000-38889200	Flanking Active TSS	Brain Substantia Nigra	brain
18	chr14:38889000-38889400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr14:38889000-38889400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr14:38889000-38889800	Enhancers	Muscle Satellite Cultured Cells	--

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