Variant report

Variant	rs35866728
Chromosome Location	chr7:41052212-41052213
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10486701	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11975144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12111891	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58118439	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73688224	0.98[AFR][1000 genomes];0.83[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	nsv5714	chr7:41026022-41059813	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:41047800-41052800	Weak transcription	NH-A	brain
2	chr7:41048600-41065600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:41049800-41053200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:41051000-41052800	Weak transcription	Osteobl	bone
5	chr7:41051000-41060400	Weak transcription	HSMMtube	muscle
6	chr7:41052200-41052400	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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