Variant report

Variant	rs186523217
Chromosome Location	chr2:151035778-151035779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005441	chr2:150457624-151060247	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv995119	chr2:150556150-151294696	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1001838	chr2:150819672-151745876	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
4	nsv535980	chr2:150819672-151745876	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
5	nsv469524	chr2:150927500-151076920	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv834412	chr2:151014270-151116638	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv583294	chr2:151022044-151037893	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv2967	chr2:151026829-151039101	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3515821	chr2:151029906-151037204	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv583297	chr2:151029978-151038142	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3515822	chr2:151030431-151037079	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3515823	chr2:151030431-151037079	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3459823	chr2:151031001-151038353	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3529254	chr2:151031025-151038354	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3529256	chr2:151031029-151039178	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3529252	chr2:151031039-151038330	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3459824	chr2:151031044-151038333	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3529255	chr2:151031055-151038286	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv961758	chr2:151031064-151038117	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3529253	chr2:151031070-151038293	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv498939	chr2:151031137-151038249	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv3459825	chr2:151031139-151038247	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3529257	chr2:151031139-151038247	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
24	esv21097	chr2:151031148-151038204	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv441789	chr2:151031451-151037730	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
26	esv1793240	chr2:151031451-151037732	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
27	esv2421344	chr2:151031451-151037732	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv583301	chr2:151033471-151035794	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	nsv583302	chr2:151033471-151037976	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
30	nsv583303	chr2:151033471-151038056	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
31	nsv583304	chr2:151033471-151038142	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	nsv583306	chr2:151033586-151037732	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv583307	chr2:151033586-151037976	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
34	nsv583308	chr2:151033586-151038142	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
35	nsv583309	chr2:151033650-151038142	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
36	nsv583310	chr2:151033721-151038142	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
37	nsv583311	chr2:151034884-151038142	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
38	nsv583312	chr2:151034931-151037976	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
39	nsv583313	chr2:151034931-151038142	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
40	nsv583314	chr2:151035328-151038142	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
41	nsv583315	chr2:151035551-151038142	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151034800-151035800	Enhancers	Liver	Liver
2	chr2:151034800-151035800	Enhancers	Fetal Intestine Large	intestine
3	chr2:151034800-151035800	Enhancers	Hela-S3	cervix
4	chr2:151035200-151035800	Enhancers	Fetal Lung	lung
5	chr2:151035400-151035800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:151035400-151047000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:151035600-151035800	Enhancers	Fetal Intestine Small	intestine
8	chr2:151035600-151035800	Enhancers	A549	lung

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