Variant report

Variant	rs187982337
Chromosome Location	chr6:133062996-133062997
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	nsv517934	chr6:133062916-133072650	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 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	chr6:133055200-133064800	Weak transcription	Primary T cells from cord blood	blood
3	chr6:133056800-133067400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:133057600-133069200	Weak transcription	GM12878-XiMat	blood
5	chr6:133058400-133064800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:133058400-133070400	Weak transcription	Liver	Liver
7	chr6:133058800-133067600	Weak transcription	Placenta	Placenta
8	chr6:133061400-133098000	Weak transcription	Spleen	Spleen
9	chr6:133061600-133072200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr6:133062000-133063000	Genic enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:133062000-133063000	Genic enhancers	Monocytes-CD14+_RO01746	blood
12	chr6:133062000-133063200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
13	chr6:133062200-133063000	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
14	chr6:133062600-133063000	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr6:133062600-133063200	Genic enhancers	Primary B cells from cord blood	blood
16	chr6:133062600-133070400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:133062800-133063200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:133062800-133065600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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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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