Variant report

Variant	rs543546456
Chromosome Location	chr6:132997066-132997067
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
3	esv275102	chr6:132996676-133001465	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132991400-132997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:132993200-133002200	Weak transcription	Liver	Liver
3	chr6:132994400-132997600	Weak transcription	Small Intestine	intestine
4	chr6:132995200-132997400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:132995400-132998600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:132996200-132998400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:132996400-132997400	Weak transcription	Primary B cells from cord blood	blood
8	chr6:132996800-132997200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr6:132996800-132997800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr6:132997000-132997200	Enhancers	Fetal Intestine Large	intestine
11	chr6:132997000-132997400	Enhancers	Duodenum Mucosa	Duodenum
12	chr6:132997000-132997800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr6:132997000-132997800	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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