Variant report

Variant	rs73106041
Chromosome Location	chr20:41766716-41766717
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs16987821	1.00[ASN][1000 genomes]
rs2867652	1.00[ASN][1000 genomes]
rs2867653	1.00[ASN][1000 genomes]
rs4516501	0.93[ASN][1000 genomes]
rs4812674	1.00[ASN][1000 genomes]
rs6016965	0.89[ASN][1000 genomes]
rs6030666	0.89[ASN][1000 genomes]
rs6073000	1.00[ASN][1000 genomes]
rs73106034	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73106039	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs869887	1.00[ASN][1000 genomes]
rs947201	1.00[ASN][1000 genomes]
rs947202	1.00[ASN][1000 genomes]
rs947203	1.00[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	nsv1063450	chr20:41409901-41880620	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1060690	chr20:41413369-41851935	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1066088	chr20:41417205-42060036	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv2751914	chr20:41744586-41890453	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr20:41763800-41767000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr20:41764200-41767400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr20:41764800-41771400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr20:41766200-41767200	Enhancers	Brain Anterior Caudate	brain
5	chr20:41766200-41767600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr20:41766200-41769200	Enhancers	Brain Substantia Nigra	brain
7	chr20:41766400-41767200	Enhancers	Brain Cingulate Gyrus	brain
8	chr20:41766400-41767400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr20:41766400-41767600	Enhancers	Brain Hippocampus Middle	brain
10	chr20:41766600-41767000	Enhancers	Placenta	Placenta
11	chr20:41766600-41768200	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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