Variant report

Variant	rs62576305
Chromosome Location	chr9:104440374-104440375
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1016429	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1323413	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1337679	0.92[ASN][1000 genomes]
rs16920640	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2224767	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28397028	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35994821	0.86[EUR][1000 genomes]
rs4742819	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56257997	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62576306	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6415854	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6479061	0.92[ASN][1000 genomes]
rs7026897	0.92[ASN][1000 genomes]
rs7469637	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7854314	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 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	chr9:104440000-104441800	Enhancers	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