Variant report

Variant	rs38266
Chromosome Location	chr7:14307871-14307872
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10263173	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12536803	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12536819	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17710027	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35198760	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36095426	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38261	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs38263	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs38264	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs38265	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs38267	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs38268	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs38269	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs38270	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs38271	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs38272	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs38275	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs38276	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs38277	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs38278	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs38284	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38285	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38286	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38287	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38289	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38290	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs40236	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs40450	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs40540	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4719396	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4721316	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6966405	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6976083	0.81[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14303800-14310000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:14306000-14309800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr7:14306000-14310400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr7:14306000-14310600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr7:14307000-14308600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:14307000-14311000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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