Variant report

Variant	rs77496163
Chromosome Location	chr4:187214087-187214088
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028146	chr4:186503899-187338335	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv530178	chr4:186659940-187478310	Bivalent Enhancer 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	26 gene(s)	inside rSNPs	diseases
3	nsv931977	chr4:186912987-187364756	Active TSS Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1033203	chr4:186990348-187333476	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv537431	chr4:186990348-187333476	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv461864	chr4:187006806-187257004	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
7	nsv596392	chr4:187006806-187257004	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv461865	chr4:187072383-187366649	Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats 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	17 gene(s)	inside rSNPs	diseases
9	nsv596401	chr4:187072383-187366649	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	esv3504560	chr4:187212808-187215806	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
11	esv2505993	chr4:187213139-187215217	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
12	esv3439308	chr4:187213258-187215656	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
13	esv3504559	chr4:187213315-187215174	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
14	nsv513190	chr4:187213455-187215306	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
15	esv2100481	chr4:187213759-187214846	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
16	esv3504558	chr4:187213779-187214882	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
17	nsv822891	chr4:187213792-187214542	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
18	esv3467515	chr4:187213812-187214846	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
19	esv3504557	chr4:187213824-187214838	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
20	esv3504562	chr4:187213840-187214791	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
21	esv3407349	chr4:187213862-187214809	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
22	esv3504561	chr4:187213884-187214866	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
23	esv3467516	chr4:187213911-187214808	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
24	esv996355	chr4:187213943-187214723	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
25	esv3504564	chr4:187213950-187214752	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
26	esv3467517	chr4:187213962-187214753	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
27	esv1700178	chr4:187213969-187214752	Weak transcription	lncRNA	n/a	inside rSNPs	diseases
28	esv1001526	chr4:187214012-187214901	Weak transcription	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187205800-187217400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:187209800-187217600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr4:187212600-187219000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:187213600-187217600	Weak transcription	Liver	Liver

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