Variant report

Variant	rs296708
Chromosome Location	chr9:93738070-93738071
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1380950	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1380951	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1380952	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs296690	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs296693	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs296696	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs296710	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs296714	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs296715	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs296716	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs296717	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs296718	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs296721	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][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	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93730400-93741600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:93733200-93738200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:93736400-93740400	Enhancers	Dnd41	blood
4	chr9:93737000-93738800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:93737000-93741000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:93737000-93741000	Weak transcription	NHEK	skin
7	chr9:93737400-93741200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:93737600-93740800	Weak transcription	HMEC	breast
9	chr9:93737600-93741400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr9:93738000-93738200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr9:93738000-93741400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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