Variant report

Variant	rs73262449
Chromosome Location	chr5:147711115-147711116
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs57705155	1.00[AMR][1000 genomes]
rs57729253	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs58096503	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6580547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6860471	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73262447	1.00[AMR][1000 genomes]
rs73262479	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7707995	1.00[AMR][1000 genomes]

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	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv599945	chr5:147649181-147720487	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr5:147709400-147749200	Weak transcription	Psoas Muscle	Psoas
2	chr5:147710000-147711200	Weak transcription	Fetal Heart	heart
3	chr5:147710600-147712600	Weak transcription	Aorta	Aorta
4	chr5:147710800-147712600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:147711000-147711600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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