Variant report

Variant	rs558429713
Chromosome Location	chr14:21660932-21660933
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:21659836..21662080-chr14:21664452..21667045,3	MCF-7	breast:
2	chr14:21659338..21661906-chr14:21661938..21664120,2	MCF-7	breast:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1048032	chr14:21602341-21847247	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	nsv541978	chr14:21602341-21847247	Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv901477	chr14:21625262-21750308	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	nsv901478	chr14:21626497-21750308	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv974434	chr14:21634973-21678548	Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS 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	9 gene(s)	inside rSNPs	diseases
15	nsv974312	chr14:21652582-21678548	Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
16	nsv1037590	chr14:21659344-21708852	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
17	nsv1044822	chr14:21659344-21860081	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21659400-21661000	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr14:21659400-21661000	Flanking Active TSS	Dnd41	blood
3	chr14:21659600-21661000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:21659600-21661000	Enhancers	Lung	lung
5	chr14:21660000-21661000	Enhancers	Placenta	Placenta
6	chr14:21660000-21661000	Enhancers	Spleen	Spleen
7	chr14:21660200-21661000	Active TSS	H9 Cell Line	embryonic stem cell
8	chr14:21660200-21661600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:21660400-21661000	Enhancers	Primary B cells from cord blood	blood
10	chr14:21660400-21661000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr14:21660400-21661000	Enhancers	GM12878-XiMat	blood
12	chr14:21660400-21661000	Flanking Bivalent TSS/Enh	HepG2	liver
13	chr14:21660400-21662000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr14:21660600-21661000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:21660600-21661000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr14:21660600-21661000	Enhancers	Primary B cells from peripheral blood	blood
17	chr14:21660600-21661000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:21660600-21661000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr14:21660600-21661000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr14:21660600-21661000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr14:21660600-21661000	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr14:21660600-21661000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:21660600-21661000	Enhancers	Fetal Thymus	thymus
24	chr14:21660600-21661000	Enhancers	Thymus	Thymus
25	chr14:21660600-21661400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:21660600-21661400	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr14:21660600-21661600	Enhancers	Esophagus	oesophagus
28	chr14:21660600-21661800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr14:21660600-21662000	Weak transcription	Ovary	ovary
30	chr14:21660600-21670000	Weak transcription	HSMMtube	muscle
31	chr14:21660600-21670200	Weak transcription	NH-A	brain
32	chr14:21660600-21673200	Weak transcription	Psoas Muscle	Psoas
33	chr14:21660600-21686200	Weak transcription	Right Atrium	heart
34	chr14:21660800-21661000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr14:21660800-21661000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
36	chr14:21660800-21661000	Enhancers	Primary T cells from cord blood	blood
37	chr14:21660800-21661000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr14:21660800-21661000	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr14:21660800-21661000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr14:21660800-21661000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:21660800-21661000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:21660800-21661000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:21660800-21661000	Active TSS	Adipose Nuclei	Adipose
44	chr14:21660800-21661000	Enhancers	Brain Angular Gyrus	brain
45	chr14:21660800-21661000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr14:21660800-21661000	Enhancers	Duodenum Mucosa	Duodenum
47	chr14:21660800-21661000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr14:21660800-21661000	Bivalent Enhancer	Fetal Intestine Large	intestine
49	chr14:21660800-21661000	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr14:21660800-21661000	Active TSS	Stomach Smooth Muscle	stomach

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