Variant report

Variant	rs373302018
Chromosome Location	chr19:56914161-56914162
allele	-/AA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:56902006..56908060-chr19:56909612..56917978,15	K562	blood:
2	chr19:56824960..56826803-chr19:56913604..56915630,2	K562	blood:
3	chr19:56902257..56906485-chr19:56913118..56917978,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF582-1	chr19:56914145-56915302	NONHSAT068149

Variant related genes	Relation type
ENSG00000266631	Chromatin interaction
ENSG00000267549	Chromatin interaction
ENSG00000131848	Chromatin interaction
ENSG00000018869	Chromatin interaction
ENSG00000267454	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
2	nsv949121	chr19:56754719-57591038	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
3	nsv1062341	chr19:56794070-57273332	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
4	nsv544094	chr19:56794070-57273332	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
5	nsv1056713	chr19:56799151-57265682	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv544095	chr19:56799151-57265682	Strong transcription ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv544096	chr19:56905651-56933455	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
8	esv3373403	chr19:56913940-56918638	Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56905600-56914600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:56905800-56914400	Weak transcription	Fetal Heart	heart
3	chr19:56908000-56914800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:56908200-56914600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:56910000-56914200	ZNF genes & repeats	Dnd41	blood
6	chr19:56910400-56914600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
7	chr19:56910600-56914200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr19:56910600-56914200	Weak transcription	Brain Anterior Caudate	brain
9	chr19:56910600-56914400	Weak transcription	Brain Substantia Nigra	brain
10	chr19:56910600-56914400	Weak transcription	Fetal Brain Male	brain
11	chr19:56910800-56914400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr19:56910800-56914600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:56911000-56914200	Weak transcription	Brain Angular Gyrus	brain
14	chr19:56911000-56914400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:56911000-56914400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr19:56911000-56914600	Weak transcription	Ovary	ovary
17	chr19:56911000-56914600	Weak transcription	Right Ventricle	heart
18	chr19:56911000-56914800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr19:56911000-56915000	Weak transcription	Aorta	Aorta
20	chr19:56911200-56914400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr19:56911400-56914200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:56912000-56914200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr19:56912000-56914200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr19:56912000-56914400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr19:56912000-56914400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:56912000-56914400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr19:56912000-56914400	Weak transcription	Brain Germinal Matrix	brain
28	chr19:56912000-56914400	Weak transcription	Brain Hippocampus Middle	brain
29	chr19:56912000-56914400	Weak transcription	Fetal Lung	lung
30	chr19:56912200-56914400	Weak transcription	Fetal Kidney	kidney
31	chr19:56912200-56914400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr19:56912200-56914600	Weak transcription	Left Ventricle	heart
33	chr19:56913000-56914200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr19:56913000-56914200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr19:56913400-56914200	Weak transcription	Primary T cells from cord blood	blood
36	chr19:56913400-56914200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr19:56913400-56914200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr19:56913400-56914200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr19:56913400-56914200	Weak transcription	HSMMtube	muscle
40	chr19:56913400-56914400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr19:56913400-56914400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr19:56913400-56914400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:56913600-56914200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr19:56913600-56914200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr19:56913600-56914200	Weak transcription	Liver	Liver
46	chr19:56913600-56914400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr19:56913600-56914400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr19:56913600-56914400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr19:56913600-56914400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr19:56913600-56914600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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