Variant report

Variant	rs79756903
Chromosome Location	chr14:65607265-65607266
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	chr14:65600313..65602525-chr14:65607232..65610149,2	MCF-7	breast:
2	chr14:65600572..65603233-chr14:65606608..65608580,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	esv1833060	chr14:65594460-65607642	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv989058	chr14:65601785-65607798	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3530651	chr14:65604499-65609897	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv564910	chr14:65604728-65607752	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv564911	chr14:65604728-65607817	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3529456	chr14:65605199-65609197	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3529457	chr14:65605199-65609197	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3426379	chr14:65605749-65609447	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3530649	chr14:65605997-65608335	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3530650	chr14:65606219-65608192	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3530648	chr14:65606313-65608116	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3530652	chr14:65606358-65608057	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv13903	chr14:65606570-65607919	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv564912	chr14:65606598-65607318	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv564913	chr14:65606598-65607376	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv564914	chr14:65606598-65607534	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv1825721	chr14:65606598-65607642	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv564915	chr14:65606598-65607642	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv564916	chr14:65606598-65607752	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1826621	chr14:65606598-65607817	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv1832042	chr14:65606598-65607817	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv564917	chr14:65606598-65607817	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv564918	chr14:65606649-65607376	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv564919	chr14:65606649-65607642	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
26	nsv564920	chr14:65606649-65607752	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv564921	chr14:65606708-65607642	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv564922	chr14:65606708-65607817	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
29	nsv564923	chr14:65606760-65607479	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
30	nsv564924	chr14:65606760-65607534	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
31	nsv564925	chr14:65606760-65607642	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
32	nsv564926	chr14:65606760-65607752	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
33	nsv564927	chr14:65606760-65607817	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
34	nsv564928	chr14:65606812-65607642	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
35	nsv564929	chr14:65606812-65607752	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
36	nsv564930	chr14:65606812-65607817	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
37	nsv564931	chr14:65607148-65607752	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65605000-65609200	Weak transcription	Osteobl	bone
2	chr14:65605400-65608800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr14:65605400-65609000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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