Variant report

Variant	rs10820918
Chromosome Location	chr9:94686453-94686454
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94676427..94678807-chr9:94685179..94687567,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10118792	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10124760	0.98[ASN][1000 genomes]
rs11795130	0.82[ASN][1000 genomes]
rs12685595	0.92[ASN][1000 genomes]
rs1881391	0.99[ASN][1000 genomes]
rs6479383	0.81[EUR][1000 genomes]
rs6479387	0.99[ASN][1000 genomes]
rs7853136	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv530946	chr9:94633154-94715023	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94678200-94686600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:94681400-94691400	Weak transcription	Pancreas	Pancrea
3	chr9:94683000-94687200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr9:94683600-94691800	Weak transcription	Fetal Lung	lung
5	chr9:94683600-94692000	Weak transcription	K562	blood
6	chr9:94684200-94686600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:94685200-94686800	Enhancers	Rectal Smooth Muscle	rectum
8	chr9:94685400-94690400	Weak transcription	Fetal Intestine Small	intestine
9	chr9:94685600-94686800	Genic enhancers	Fetal Stomach	stomach
10	chr9:94685800-94686600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr9:94686000-94686600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:94686000-94686600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:94686000-94686600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:94686000-94686600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:94686200-94686600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr9:94686200-94686600	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr9:94686200-94686600	Enhancers	Gastric	stomach
18	chr9:94686200-94686600	Enhancers	Ovary	ovary
19	chr9:94686400-94686600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
20	chr9:94686400-94686600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr9:94686400-94686600	Enhancers	Esophagus	oesophagus
22	chr9:94686400-94689200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:94686400-94692400	Weak transcription	Colon Smooth Muscle	Colon

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