Variant report

Variant	rs73644244
Chromosome Location	chr9:18564315-18564316
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11788108	0.90[EUR][1000 genomes]
rs11789251	0.90[EUR][1000 genomes]
rs11791689	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11794207	0.85[EUR][1000 genomes]
rs11795292	0.90[EUR][1000 genomes]
rs55686384	0.81[EUR][1000 genomes]
rs56083866	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60993688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61364591	0.87[EUR][1000 genomes]
rs7031043	0.87[EUR][1000 genomes]
rs73644243	0.92[AFR][1000 genomes]
rs73644246	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv892690	chr9:18485434-18592374	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv428536	chr9:18512807-18667760	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
9	nsv892691	chr9:18519699-18805483	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv892693	chr9:18541710-18584860	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18546200-18564600	Weak transcription	NH-A	brain
2	chr9:18546200-18574000	Weak transcription	Fetal Heart	heart
3	chr9:18550200-18564400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:18555800-18564800	Weak transcription	HUVEC	blood vessel
5	chr9:18563400-18564400	ZNF genes & repeats	Fetal Stomach	stomach
6	chr9:18563600-18564400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr9:18563600-18565800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr9:18563600-18569400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:18563800-18564400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr9:18563800-18564400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:18564000-18564400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:18564000-18564400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:18564000-18564400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:18564000-18564400	Enhancers	Esophagus	oesophagus
15	chr9:18564000-18564600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:18564200-18564400	Enhancers	Aorta	Aorta
17	chr9:18564200-18565600	Genic enhancers	HSMM	muscle
18	chr9:18564200-18566400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:18564200-18567000	Enhancers	NHDF-Ad	bronchial
20	chr9:18564200-18567000	Enhancers	Osteobl	bone

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