Variant report

Variant	rs12227581
Chromosome Location	chr12:30037997-30037998
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10431222	0.91[EUR][1000 genomes]
rs10431276	0.90[EUR][1000 genomes]
rs10771589	0.84[EUR][1000 genomes]
rs10771590	0.89[EUR][1000 genomes]
rs10771591	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10771592	0.89[EUR][1000 genomes]
rs10843527	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10843528	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10843529	0.91[EUR][1000 genomes]
rs10843531	0.94[ASN][1000 genomes]
rs10843537	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10843538	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10843539	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11050509	0.90[EUR][1000 genomes]
rs11050511	0.91[ASN][1000 genomes]
rs11050521	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11050523	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12226994	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12227846	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12227886	0.98[ASN][1000 genomes]
rs12229602	0.91[EUR][1000 genomes]
rs2062292	0.91[EUR][1000 genomes]
rs2129137	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2129140	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2351015	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2351035	0.80[AMR][1000 genomes]
rs4622345	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57237787	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58304678	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59181833	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7133046	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7135043	0.91[EUR][1000 genomes]
rs7299824	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7302158	0.91[EUR][1000 genomes]
rs7307169	0.89[EUR][1000 genomes]
rs7952895	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7958365	0.89[EUR][1000 genomes]
rs7973763	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[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	chr12:30036000-30038200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr12:30036000-30038600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:30036800-30039200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:30037000-30039400	Weak transcription	Fetal Heart	heart
5	chr12:30037400-30039000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr12:30037600-30038400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:30037800-30049400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links