Variant report

Variant	rs115592516
Chromosome Location	chr5:93256822-93256823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532196	chr5:92933949-93573527	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv830405	chr5:93086825-93258518	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv882384	chr5:93136661-93380123	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1028893	chr5:93213264-93276883	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1020849	chr5:93228065-93279216	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1030870	chr5:93242611-93282996	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv980573	chr5:93255694-93260934	Flanking Active TSS Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:93194200-93307600	Weak transcription	Left Ventricle	heart
2	chr5:93226800-93269600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr5:93228000-93266600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr5:93249600-93261000	Weak transcription	NHDF-Ad	bronchial
5	chr5:93250000-93262200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:93250200-93273800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr5:93250800-93259200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr5:93252200-93284400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr5:93253000-93259000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:93253200-93263200	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr5:93255800-93258200	Enhancers	Fetal Thymus	thymus
12	chr5:93256200-93259600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr5:93256400-93257200	Strong transcription	Primary B cells from cord blood	blood
14	chr5:93256400-93258000	Flanking Active TSS	Dnd41	blood
15	chr5:93256800-93258000	Enhancers	Thymus	Thymus

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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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