Variant report

Variant	rs11206626
Chromosome Location	chr1:56058491-56058492
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1039294	0.84[CEU][hapmap]
rs10493193	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10493194	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10493195	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs11206627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11206635	0.92[CEU][hapmap];0.98[EUR][1000 genomes]
rs11206649	0.85[CEU][hapmap]
rs1165460	0.89[CHB][hapmap]
rs11801001	0.92[CEU][hapmap]
rs11805740	0.92[CEU][hapmap];0.98[EUR][1000 genomes]
rs12059018	0.92[ASN][1000 genomes]
rs12071564	0.89[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs12081733	0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs12088041	0.89[CHB][hapmap];0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs12116670	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs12117758	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs12125730	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs12139482	1.00[CEU][hapmap]
rs17112410	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17112413	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17418048	0.85[CEU][hapmap]
rs17418151	0.85[CEU][hapmap]
rs17452287	0.85[CEU][hapmap]
rs1846562	0.98[EUR][1000 genomes]
rs1846563	0.95[EUR][1000 genomes]
rs59236443	0.95[ASN][1000 genomes]
rs59539072	0.95[ASN][1000 genomes]
rs60149406	0.95[ASN][1000 genomes]
rs61566671	0.97[EUR][1000 genomes]
rs6588567	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6670673	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6677373	0.88[CHB][hapmap];0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs6680818	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6681925	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6694680	0.98[EUR][1000 genomes]
rs6694786	0.92[CEU][hapmap];0.98[EUR][1000 genomes]
rs7519540	0.85[CEU][hapmap]
rs7520444	0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7548272	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7549716	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs7550575	0.84[CEU][hapmap]
rs769970	0.97[EUR][1000 genomes]
rs769989	1.00[CEU][hapmap];0.98[EUR][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	nsv10184	chr1:55728755-56084833	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv523489	chr1:56038407-56066503	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv461617	chr1:56055190-56123510	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv546303	chr1:56055190-56123510	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56040600-56058600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr1:56052800-56060400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:56054400-56059000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:56056000-56066000	Weak transcription	Fetal Lung	lung
5	chr1:56056200-56062400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:56057200-56058800	Enhancers	Fetal Heart	heart
7	chr1:56057200-56059200	Enhancers	Right Atrium	heart
8	chr1:56058000-56058600	Enhancers	Aorta	Aorta
9	chr1:56058000-56059800	Enhancers	Fetal Stomach	stomach

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