Variant report

Variant	rs181621532
Chromosome Location	chr13:65356744-65356745
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455914	chr13:64432922-65368490	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv561965	chr13:64432922-65368490	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3367739	chr13:64805577-65549276	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1042755	chr13:65300441-65400043	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv561978	chr13:65339575-65360698	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv561979	chr13:65339575-65366000	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv561996	chr13:65342539-65360698	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
8	nsv561997	chr13:65342539-65360737	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
9	nsv562011	chr13:65342591-65360698	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
10	nsv562023	chr13:65342642-65360698	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
11	nsv562050	chr13:65342863-65360698	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
12	nsv562061	chr13:65343028-65360698	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
13	nsv562073	chr13:65352237-65360698	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	nsv562078	chr13:65352317-65360698	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	nsv562084	chr13:65352656-65360698	Enhancers Weak transcription	n/a	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	chr13:65356600-65356800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:65356600-65357600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr13:65356600-65357800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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