Variant report

Variant	rs9332578
Chromosome Location	chr1:169526020-169526021
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs3917745	1.00[AMR][1000 genomes]
rs3917845	1.00[AMR][1000 genomes]
rs9332572	1.00[AMR][1000 genomes]
rs9332622	1.00[AMR][1000 genomes]
rs9332626	1.00[AMR][1000 genomes]
rs9332632	1.00[AMR][1000 genomes]
rs9332648	1.00[AMR][1000 genomes]
rs9332663	1.00[AMR][1000 genomes]
rs9332675	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169500200-169526800	Weak transcription	Left Ventricle	heart
2	chr1:169505800-169534800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr1:169506200-169542800	Weak transcription	Right Ventricle	heart
4	chr1:169507000-169530800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:169516000-169531400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:169517200-169530400	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr1:169518000-169531000	Strong transcription	HepG2	liver
8	chr1:169518400-169531000	Strong transcription	Liver	Liver
9	chr1:169523000-169530200	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:169523000-169530800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:169524600-169526200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:169524600-169541800	Weak transcription	Placenta	Placenta
13	chr1:169525400-169527000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:169525400-169528000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr1:169525800-169526600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:169525800-169526600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr1:169525800-169527000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:169525800-169527400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:169526000-169527000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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