Variant report

Variant	rs12914590
Chromosome Location	chr15:58320780-58320781
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10851630	0.82[AFR][1000 genomes]
rs10851633	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11071356	0.80[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs11071365	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11071366	0.91[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11630835	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11631127	0.82[AFR][1000 genomes]
rs11852540	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11855259	0.87[AFR][1000 genomes]
rs11857461	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12148093	0.93[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12148907	0.94[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12898976	0.81[AFR][1000 genomes]
rs12901462	0.93[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12903474	0.93[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12903551	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs12908953	0.93[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12910752	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12911071	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12915693	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12915901	0.98[ASN][1000 genomes]
rs1372368	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs3204689	0.84[AFR][1000 genomes]
rs34871384	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs35246600	0.91[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs35511675	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4369598	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4646563	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4646568	0.98[ASN][1000 genomes]
rs4646571	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4646572	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4646576	0.91[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4646586	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4646593	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4646596	0.80[AFR][1000 genomes]
rs4646600	0.83[AFR][1000 genomes]
rs4646611	0.90[ASN][1000 genomes]
rs4646612	0.90[ASN][1000 genomes]
rs4646619	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4646622	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4646627	0.85[AFR][1000 genomes]
rs4646629	0.85[AFR][1000 genomes]
rs4646638	0.85[AFR][1000 genomes]
rs4646640	0.84[AFR][1000 genomes]
rs7164408	0.83[ASN][1000 genomes]
rs7178497	0.82[AFR][1000 genomes]
rs8031133	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8032107	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8032572	0.81[AFR][1000 genomes]
rs9325	0.87[AFR][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	nsv1038667	chr15:57933076-58481870	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv542400	chr15:57933076-58481870	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv833023	chr15:58161839-58340174	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv904261	chr15:58258424-58347260	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58318800-58323800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:58319000-58325000	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links