Variant report

Variant	rs73513326
Chromosome Location	chr9:118395338-118395339
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs59671136	0.81[AFR][1000 genomes]
rs7021225	1.00[AFR][1000 genomes]
rs73513311	0.82[AFR][1000 genomes]
rs73513318	0.85[AFR][1000 genomes]
rs73513350	1.00[AFR][1000 genomes]
rs73515310	0.88[AFR][1000 genomes]
rs73516421	0.83[AFR][1000 genomes]
rs73517510	0.88[AFR][1000 genomes]
rs73517513	0.88[AFR][1000 genomes]
rs73517526	0.88[AFR][1000 genomes]
rs73528138	0.83[AFR][1000 genomes]
rs73528139	0.83[AFR][1000 genomes]
rs73528142	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv948346	chr9:118107565-118718197	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1046948	chr9:118185587-118926891	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv916622	chr9:118206309-118952390	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv540207	chr9:118206311-118920304	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv491661	chr9:118206312-118802177	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv831698	chr9:118284259-118446456	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1047164	chr9:118286742-118456851	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118390800-118398800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr9:118393400-118399800	Weak transcription	NHLF	lung
3	chr9:118394600-118396000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:118394600-118397000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:118394800-118395600	Enhancers	Esophagus	oesophagus
6	chr9:118394800-118395600	Enhancers	Stomach Smooth Muscle	stomach
7	chr9:118394800-118395800	Enhancers	Aorta	Aorta
8	chr9:118394800-118395800	Enhancers	NHEK	skin
9	chr9:118394800-118396000	Enhancers	HMEC	breast
10	chr9:118394800-118396000	Enhancers	NH-A	brain
11	chr9:118395000-118395600	Enhancers	HSMMtube	muscle
12	chr9:118395000-118395800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:118395000-118396200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr9:118395000-118396400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr9:118395200-118395600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:118395200-118395600	Enhancers	NHDF-Ad	bronchial
17	chr9:118395200-118395800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:118395200-118395800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr9:118395200-118396000	Enhancers	HSMM	muscle
20	chr9:118395200-118396200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:118395200-118396200	Enhancers	Osteobl	bone

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