Variant report

Variant	rs560792419
Chromosome Location	chr13:76611889-76611890
allele	C/T
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	nsv832649	chr13:76424872-76657891	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1054431	chr13:76460431-76885094	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541837	chr13:76460431-76885094	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2483877	chr13:76608302-76613420	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv471735	chr13:76608545-76612872	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv2036920	chr13:76608675-76612915	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	nsv9089	chr13:76608693-76611897	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3518953	chr13:76608702-76612872	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3518964	chr13:76608863-76612759	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv13831	chr13:76609091-76612717	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3693151	chr13:76610127-76612357	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv818981	chr13:76610127-76612357	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv2421663	chr13:76610127-76612755	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv516991	chr13:76610127-76634901	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv455988	chr13:76610561-76662923	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv562363	chr13:76610561-76662923	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv2760297	chr13:76610840-76612996	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	nsv442320	chr13:76611749-76612847	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76608000-76612000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr13:76609600-76613800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:76610600-76612400	Enhancers	Fetal Thymus	thymus
4	chr13:76611200-76612000	Enhancers	Thymus	Thymus
5	chr13:76611400-76613000	Weak transcription	Brain Anterior Caudate	brain
6	chr13:76611600-76612200	Weak transcription	Fetal Lung	lung
7	chr13:76611800-76613200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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