Variant report

Variant	rs148141439
Chromosome Location	chr14:45607465-45607466
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr14:45607186-45607470	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45603146..45606664-chr14:45606745..45609948,6	MCF-7	breast:
2	chr14:45428929..45435608-chr14:45601966..45608462,12	MCF-7	breast:
3	chr14:45601512..45605313-chr14:45605494..45608093,6	K562	blood:
4	chr14:45600775..45605834-chr14:45607431..45611467,5	K562	blood:

Variant related genes	Relation type
FKBP3	TF binding region
ENSG00000100442	Chromatin interaction
ENSG00000198718	Chromatin interaction
ENSG00000179454	Chromatin interaction
ENSG00000187790	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901841	chr14:45198196-45719643	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv1795667	chr14:45361680-45721052	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv1794986	chr14:45368685-45650813	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv1803131	chr14:45441932-45726848	Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv933364	chr14:45467086-45705844	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv901842	chr14:45506857-45713358	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv901843	chr14:45506857-45833490	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	nsv832785	chr14:45520670-45710741	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	esv1800510	chr14:45572528-45650813	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv530814	chr14:45604432-46198418	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv901844	chr14:45606287-46063731	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv1044445	chr14:45606779-45807171	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45600600-45608600	Active TSS	GM12878-XiMat	blood
2	chr14:45602000-45608200	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr14:45602200-45607600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:45602200-45607600	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr14:45602200-45608000	Active TSS	K562	blood
6	chr14:45602800-45608000	Active TSS	NHDF-Ad	bronchial
7	chr14:45605800-45613800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:45605800-45613800	Weak transcription	Gastric	stomach
9	chr14:45605800-45613800	Weak transcription	Lung	lung
10	chr14:45605800-45618200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:45606000-45608200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr14:45606000-45608200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr14:45606000-45614000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr14:45606000-45618400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr14:45606000-45618600	Weak transcription	Left Ventricle	heart
16	chr14:45606000-45618800	Weak transcription	Placenta	Placenta
17	chr14:45606000-45622200	Weak transcription	Pancreas	Pancrea
18	chr14:45606000-45634600	Weak transcription	Esophagus	oesophagus
19	chr14:45606000-45679600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr14:45606200-45607600	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr14:45606200-45608800	Flanking Active TSS	Dnd41	blood
22	chr14:45606200-45622400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:45606400-45607600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr14:45606400-45607800	Enhancers	Primary T cells from cord blood	blood
25	chr14:45606400-45613800	Weak transcription	Spleen	Spleen
26	chr14:45606400-45615800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr14:45606400-45616000	Weak transcription	Right Ventricle	heart
28	chr14:45606400-45620600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr14:45606400-45641200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr14:45606600-45607600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr14:45606600-45607600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:45606600-45608200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:45606600-45608400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr14:45606600-45630600	Weak transcription	Fetal Muscle Leg	muscle
35	chr14:45606600-45634400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr14:45606600-45636400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr14:45606800-45607600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:45606800-45607600	Enhancers	Primary hematopoietic stem cells	blood
39	chr14:45606800-45607600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr14:45607000-45607600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr14:45607000-45608400	Enhancers	Brain Germinal Matrix	brain
42	chr14:45607000-45613600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:45607000-45613800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr14:45607000-45613800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:45607000-45636400	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr14:45607000-45660000	Weak transcription	Ovary	ovary
47	chr14:45607200-45607800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr14:45607200-45608000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr14:45607200-45609000	Enhancers	Osteobl	bone
50	chr14:45607200-45613600	Weak transcription	Fetal Stomach	stomach

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