Variant report

Variant	rs397853232
Chromosome Location	chr14:32366395-32366396
allele	-/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	nsv564180	chr14:31958566-32368934	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv564182	chr14:32110519-32584337	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1046526	chr14:32110537-32567426	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv526200	chr14:32308511-32454372	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv519917	chr14:32363980-32375359	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2760330	chr14:32364547-32377760	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1040337	chr14:32364547-32387656	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32358800-32366600	Weak transcription	Fetal Brain Female	brain
2	chr14:32363000-32366800	Weak transcription	Fetal Lung	lung
3	chr14:32363800-32366400	Weak transcription	Brain Germinal Matrix	brain
4	chr14:32363800-32367000	Weak transcription	Fetal Heart	heart
5	chr14:32364000-32367600	Weak transcription	Gastric	stomach
6	chr14:32364200-32371200	Weak transcription	Placenta	Placenta
7	chr14:32364400-32371000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr14:32364600-32366800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:32364800-32367000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:32364800-32370400	Weak transcription	K562	blood
11	chr14:32364800-32371000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr14:32365000-32366400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr14:32365000-32366600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:32365000-32366800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr14:32365200-32366400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr14:32365200-32366600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:32365200-32366800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:32365200-32368000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr14:32365200-32368000	Weak transcription	HMEC	breast
20	chr14:32365200-32370800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:32365200-32370800	Weak transcription	NHEK	skin
22	chr14:32365600-32366800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:32366000-32367200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:32366200-32367000	Enhancers	Left Ventricle	heart
25	chr14:32366200-32367200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:32366200-32367200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr14:32366200-32369000	Enhancers	Primary B cells from peripheral blood	blood

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