Variant report

Variant	rs45474194
Chromosome Location	chr20:40705873-40705874
allele	A/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:19)

rs_ID	r²[population]
rs1076666	0.80[ASN][1000 genomes]
rs1569547	0.95[ASN][1000 genomes]
rs2016647	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2866943	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35258493	0.80[EUR][1000 genomes]
rs3787279	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55683344	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6016688	0.84[ASN][1000 genomes]
rs6065432	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6072628	0.87[ASN][1000 genomes]
rs6102659	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6102662	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6102677	0.87[ASN][1000 genomes]
rs6130026	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6130031	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67506870	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs722897	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs742293	0.84[ASN][1000 genomes]
rs877431	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];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	nsv3381	chr20:39925326-40765696	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS 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 target site	34 gene(s)	inside rSNPs	diseases
2	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	esv995175	chr20:40699252-40707470	Enhancers Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:40701800-40715200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:40702800-40706000	Enhancers	Fetal Stomach	stomach
3	chr20:40703800-40713200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr20:40705400-40706000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:40705800-40707600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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

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