Variant report

Variant	rs547746950
Chromosome Location	chr6:133058290-133058291
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	nsv965662	chr6:133058111-133063853	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133044400-133066200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr6:133052400-133058800	Enhancers	Stomach Mucosa	stomach
3	chr6:133054400-133058400	Enhancers	HepG2	liver
4	chr6:133055200-133064800	Weak transcription	Primary T cells from cord blood	blood
5	chr6:133056000-133058400	Enhancers	Liver	Liver
6	chr6:133056000-133059000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:133056800-133058600	Enhancers	Primary B cells from cord blood	blood
8	chr6:133056800-133067400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr6:133057200-133058400	Enhancers	Hela-S3	cervix
10	chr6:133057400-133058400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr6:133057600-133069200	Weak transcription	GM12878-XiMat	blood
12	chr6:133057800-133058400	Enhancers	Small Intestine	intestine
13	chr6:133058000-133058400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr6:133058000-133058600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr6:133058000-133058800	Enhancers	Placenta	Placenta
16	chr6:133058200-133058600	Enhancers	Pancreas	Pancrea

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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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