Variant report

Variant	rs372379690
Chromosome Location	chr14:103934465-103934466
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049747	chr14:103126148-103955984	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
2	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
4	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv85420	chr14:103934035-103936396	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103879000-103941400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:103912200-103942200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr14:103918600-103941400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr14:103922400-103939200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:103922400-103955000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:103922800-103940800	Weak transcription	Fetal Heart	heart
7	chr14:103923000-103935800	Weak transcription	Psoas Muscle	Psoas
8	chr14:103923000-103941600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:103923000-103949400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:103923200-103938200	Strong transcription	NHEK	skin
11	chr14:103923200-103976800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr14:103923600-103967000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr14:103923800-103938400	Strong transcription	Liver	Liver
14	chr14:103923800-103941400	Weak transcription	Small Intestine	intestine
15	chr14:103924000-103957400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:103924400-103937200	Weak transcription	Stomach Mucosa	stomach
17	chr14:103925600-103958400	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:103926200-103950400	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr14:103926600-103938400	Strong transcription	HMEC	breast
20	chr14:103926800-103963400	Strong transcription	Fetal Intestine Large	intestine
21	chr14:103927200-103938400	Strong transcription	Dnd41	blood
22	chr14:103927200-103942400	Weak transcription	Fetal Brain Male	brain
23	chr14:103927400-103944200	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr14:103927400-103944800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr14:103927600-103938400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr14:103927600-103938400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr14:103927600-103944000	Strong transcription	Fetal Thymus	thymus
28	chr14:103927600-103946600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr14:103927800-103937000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr14:103927800-103938000	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:103927800-103938000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:103927800-103938000	Strong transcription	Primary B cells from peripheral blood	blood
33	chr14:103927800-103938000	Strong transcription	Fetal Muscle Trunk	muscle
34	chr14:103927800-103938200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:103927800-103938400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr14:103927800-103939600	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr14:103927800-103944400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr14:103927800-103945400	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr14:103927800-103946000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr14:103927800-103946400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:103927800-103946600	Strong transcription	Duodenum Mucosa	Duodenum
42	chr14:103927800-103949200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr14:103927800-103951000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr14:103927800-103951600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr14:103927800-103979800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr14:103928000-103938000	Strong transcription	Osteobl	bone
47	chr14:103928000-103938200	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr14:103928000-103938200	Strong transcription	Thymus	Thymus
49	chr14:103928000-103946600	Strong transcription	Primary T cells from cord blood	blood
50	chr14:103928000-103946800	Strong transcription	Fetal Intestine Small	intestine

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