Variant report

Variant	rs7996707
Chromosome Location	chr13:97811070-97811071
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs16953899	0.82[ASN][1000 genomes]
rs16953900	0.82[ASN][1000 genomes]
rs4445760	0.82[ASN][1000 genomes]
rs4456365	0.82[ASN][1000 genomes]
rs7322677	0.82[ASN][1000 genomes]
rs7322973	0.82[ASN][1000 genomes]
rs7331281	0.84[ASN][1000 genomes]
rs7332127	0.82[ASN][1000 genomes]
rs7337250	0.81[ASN][1000 genomes]
rs7338420	0.82[ASN][1000 genomes]
rs7338629	0.82[ASN][1000 genomes]
rs7983895	0.80[ASN][1000 genomes]
rs7995449	0.82[ASN][1000 genomes]
rs7997574	0.82[ASN][1000 genomes]
rs9513209	0.81[ASN][1000 genomes]
rs9513210	0.82[ASN][1000 genomes]
rs9513211	0.82[ASN][1000 genomes]
rs9516840	0.84[ASN][1000 genomes]
rs9516841	0.84[ASN][1000 genomes]
rs9516844	0.82[ASN][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	nsv1137	chr13:97803474-97848814	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:97799200-97814800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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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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