Variant report

Variant	rs9332613
Chromosome Location	chr1:169505295-169505296
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs9332605	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9332631	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9332671	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9332672	1.00[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv872533	chr1:169490401-169508576	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169485400-169510600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr1:169496000-169515200	Strong transcription	Liver	Liver
3	chr1:169498400-169524000	Weak transcription	Placenta	Placenta
4	chr1:169498600-169506200	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:169498600-169507600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:169499000-169508400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:169499000-169519000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:169500200-169526800	Weak transcription	Left Ventricle	heart
9	chr1:169503400-169507400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr1:169504000-169505800	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr1:169504000-169506000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr1:169504000-169515000	Strong transcription	HepG2	liver
13	chr1:169504200-169505400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:169504600-169505800	Strong transcription	Primary T helper cells PMA-I stimulated	--
15	chr1:169505200-169510200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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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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