Variant report

Variant	rs61770106
Chromosome Location	chr1:62193831-62193832
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12402847	1.00[ASN][1000 genomes]
rs12408315	1.00[ASN][1000 genomes]
rs12410306	1.00[ASN][1000 genomes]
rs12728331	1.00[ASN][1000 genomes]
rs2938	1.00[ASN][1000 genomes]
rs34403905	1.00[ASN][1000 genomes]
rs34473594	1.00[ASN][1000 genomes]
rs35138123	0.86[EUR][1000 genomes]
rs35180388	1.00[ASN][1000 genomes]
rs35318456	1.00[ASN][1000 genomes]
rs35722784	1.00[ASN][1000 genomes]
rs61770086	0.86[EUR][1000 genomes]
rs61770105	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs71641748	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv994970	chr1:61693951-62199657	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1000294	chr1:61746280-62350718	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62191400-62195200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:62191400-62207400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:62191600-62197000	Weak transcription	HepG2	liver

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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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