Variant report

Variant	rs56785986
Chromosome Location	chr12:122662672-122662673
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11834748	1.00[ASN][1000 genomes]
rs11837919	1.00[ASN][1000 genomes]
rs12099705	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12579871	1.00[ASN][1000 genomes]
rs12581610	1.00[ASN][1000 genomes]
rs56719421	1.00[ASN][1000 genomes]
rs57141433	1.00[ASN][1000 genomes]
rs57302703	1.00[ASN][1000 genomes]
rs58270183	1.00[ASN][1000 genomes]
rs59731700	1.00[ASN][1000 genomes]
rs61126567	1.00[ASN][1000 genomes]
rs7138188	1.00[AMR][1000 genomes]
rs7315448	1.00[ASN][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	nsv529868	chr12:121956483-122944265	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
2	nsv916686	chr12:122240149-122714056	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv527450	chr12:122481290-122676531	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv1038827	chr12:122627371-122687913	Bivalent/Poised TSS Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122658600-122667000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:122658800-122667400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:122661200-122665000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:122661400-122665000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr12:122661600-122664600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr12:122661600-122665000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:122662200-122667200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr12:122662400-122662800	Weak transcription	HepG2	liver
9	chr12:122662400-122667200	Weak transcription	Liver	Liver
10	chr12:122662400-122667200	Weak transcription	Fetal Intestine Large	intestine
11	chr12:122662400-122667200	Weak transcription	Fetal Intestine Small	intestine

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