Variant report

Variant	rs7262144
Chromosome Location	chr20:15592510-15592511
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs16996274	1.00[AMR][1000 genomes]
rs6034237	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs6034245	1.00[AMR][1000 genomes]
rs6043395	1.00[YRI][hapmap]
rs6043400	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs6043411	1.00[AMR][1000 genomes]
rs6043414	1.00[AMR][1000 genomes]
rs6043416	1.00[AMR][1000 genomes]
rs7271832	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2751909	chr20:15489871-15656007	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15584800-15593600	Weak transcription	Fetal Intestine Small	intestine
2	chr20:15589000-15596000	Enhancers	Fetal Heart	heart
3	chr20:15591000-15595200	Enhancers	Liver	Liver
4	chr20:15591600-15594400	Weak transcription	Aorta	Aorta
5	chr20:15592200-15594800	Enhancers	Fetal Lung	lung

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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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