Variant report

Variant	rs4324970
Chromosome Location	chr9:104470105-104470106
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10121600	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs10819978	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12351943	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12352862	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1407871	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1407872	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1951781	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2067056	0.81[CEU][hapmap]
rs7035242	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]

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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1046590	chr9:104450624-104848588	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104468000-104474400	Weak transcription	Pancreas	Pancrea
2	chr9:104468200-104471400	Enhancers	Fetal Lung	lung
3	chr9:104468800-104470800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:104469000-104470600	Enhancers	Adipose Nuclei	Adipose
5	chr9:104469400-104471800	Enhancers	Liver	Liver
6	chr9:104469800-104470400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:104469800-104470600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr9:104470000-104470200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr9:104470000-104470200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr9:104470000-104470600	Enhancers	iPS-20b Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links