Variant report

Variant	rs7525013
Chromosome Location	chr1:84271902-84271903
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12074234	1.00[EUR][1000 genomes]
rs17129409	1.00[EUR][1000 genomes]
rs17129477	1.00[EUR][1000 genomes]
rs17129902	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17129942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6704231	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72936219	1.00[EUR][1000 genomes]
rs7514034	0.87[AFR][1000 genomes]
rs7515975	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2133471	chr1:84271734-84272222	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3320336	chr1:84271832-84272102	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3320335	chr1:84271838-84272059	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3743	chr1:84271847-84272114	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3320337	chr1:84271888-84272039	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3320338	chr1:84271903-84272036	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84268800-84273400	Weak transcription	Adipose Nuclei	Adipose
2	chr1:84268800-84273600	Weak transcription	Liver	Liver
3	chr1:84271600-84272200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:84271800-84272200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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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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