Variant report

Variant	rs531461803
Chromosome Location	chr4:46798296-46798297
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878998	chr4:46565663-46823634	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv878999	chr4:46565663-46860626	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv461356	chr4:46635167-46846042	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv594117	chr4:46635167-46846042	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv879000	chr4:46635167-46890046	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv2450256	chr4:46796388-46799761	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv2410412	chr4:46796820-46799338	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3465240	chr4:46796877-46799245	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
9	esv3513456	chr4:46796904-46799243	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
10	esv3513455	chr4:46796920-46799219	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3513458	chr4:46796925-46799175	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3465237	chr4:46796933-46799211	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3465238	chr4:46796945-46799169	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
14	esv3513457	chr4:46796954-46799182	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
15	esv3465239	chr4:46796987-46799143	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
16	esv3513459	chr4:46796997-46799152	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3465242	chr4:46797001-46799150	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3513460	chr4:46797001-46799150	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46797000-46799200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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