Variant report

Variant	rs12307927
Chromosome Location	chr12:26056330-26056331
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12306291	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12306703	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12306760	1.00[EUR][1000 genomes]
rs12312960	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12313687	1.00[EUR][1000 genomes]
rs12318713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57032617	0.94[ASN][1000 genomes]
rs61591863	0.94[ASN][1000 genomes]
rs73289120	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73290920	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs74072243	0.94[ASN][1000 genomes]
rs74072251	0.94[ASN][1000 genomes]
rs74072252	0.94[ASN][1000 genomes]
rs74072256	0.88[ASN][1000 genomes]
rs74072257	0.86[ASN][1000 genomes]
rs74072258	0.86[ASN][1000 genomes]
rs74072261	0.86[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	esv2758300	chr12:25992331-26161116	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	esv2759886	chr12:25992331-26161116	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1035319	chr12:26020667-26097148	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26050400-26076800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:26055200-26056400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:26056200-26056400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:26056200-26057000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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