Variant report

Variant	rs12227886
Chromosome Location	chr12:30038254-30038255
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10771591	0.90[ASN][1000 genomes]
rs10843528	0.94[ASN][1000 genomes]
rs10843531	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10843539	0.98[ASN][1000 genomes]
rs11050511	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11050521	0.95[ASN][1000 genomes]
rs12226994	0.93[ASN][1000 genomes]
rs12227581	0.98[ASN][1000 genomes]
rs12227846	0.98[ASN][1000 genomes]
rs2129137	0.94[ASN][1000 genomes]
rs2351015	0.84[ASN][1000 genomes]
rs4622345	0.87[ASN][1000 genomes]
rs57237787	0.91[ASN][1000 genomes]
rs58304678	0.91[ASN][1000 genomes]
rs59181833	0.91[ASN][1000 genomes]
rs7133046	0.94[ASN][1000 genomes]
rs7973763	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529328	chr12:29692414-30246209	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv469191	chr12:29939628-30098770	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv557958	chr12:29939628-30098770	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv526146	chr12:29989292-30112823	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv2758302	chr12:30023167-30175232	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv2759889	chr12:30023167-30175232	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30036000-30038600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:30036800-30039200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:30037000-30039400	Weak transcription	Fetal Heart	heart
4	chr12:30037400-30039000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:30037600-30038400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr12:30037800-30049400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr12:30038200-30038800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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