Variant report

Variant	rs7954663
Chromosome Location	chr12:30503751-30503752
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11832986	1.00[EUR][1000 genomes]
rs12301857	0.85[AMR][1000 genomes]
rs12307190	0.91[EUR][1000 genomes]
rs12308930	0.91[EUR][1000 genomes]
rs12320822	0.91[EUR][1000 genomes]
rs12322450	0.91[EUR][1000 genomes]
rs16906339	0.92[EUR][1000 genomes]
rs16906347	1.00[EUR][1000 genomes]
rs2351920	0.91[EUR][1000 genomes]
rs3866687	0.91[EUR][1000 genomes]
rs3866688	0.91[EUR][1000 genomes]
rs3885183	0.91[EUR][1000 genomes]
rs57573513	1.00[EUR][1000 genomes]
rs57982142	1.00[EUR][1000 genomes]
rs58192678	1.00[EUR][1000 genomes]
rs58759836	1.00[EUR][1000 genomes]
rs7132701	1.00[EUR][1000 genomes]
rs73075867	0.82[EUR][1000 genomes]
rs7487093	0.91[EUR][1000 genomes]
rs7974124	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832360	chr12:30393329-30555693	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	esv11198	chr12:30496609-30508640	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2754065	chr12:30499833-30560733	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 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	chr12:30501400-30510800	Weak transcription	Fetal Heart	heart

Quick Search:

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

what's new

Quick links