Variant report

Variant	rs1711403
Chromosome Location	chr11:102456796-102456797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1615443	0.84[ASN][1000 genomes]
rs1631411	0.81[EUR][1000 genomes]
rs1632456	0.81[AFR][1000 genomes]
rs1711399	0.92[AFR][1000 genomes]
rs1711400	0.83[AFR][1000 genomes]
rs1711401	0.92[AFR][1000 genomes]
rs1711420	0.81[EUR][1000 genomes]
rs1711421	0.81[EUR][1000 genomes]
rs1711422	0.81[EUR][1000 genomes]
rs1711423	0.81[EUR][1000 genomes]
rs1711425	0.81[EUR][1000 genomes]
rs1711426	0.81[EUR][1000 genomes]
rs1711427	0.81[EUR][1000 genomes]
rs1711429	0.81[EUR][1000 genomes]
rs1711430	0.87[ASN][1000 genomes]
rs1711432	0.88[ASN][1000 genomes]
rs1711434	0.80[AFR][1000 genomes]
rs1711437	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1711438	0.81[AFR][1000 genomes]
rs1711439	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1711441	0.90[AFR][1000 genomes]
rs1711443	0.90[AFR][1000 genomes]
rs1784400	0.81[AFR][1000 genomes]
rs1784405	0.81[AFR][1000 genomes]
rs1784407	0.81[AFR][1000 genomes]
rs1784410	1.00[ASN][1000 genomes]
rs1784421	0.81[EUR][1000 genomes]
rs1784422	0.80[EUR][1000 genomes]
rs1784423	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1784424	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1784426	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1784427	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1784431	0.82[ASN][1000 genomes]
rs1784432	0.88[ASN][1000 genomes]
rs1784433	0.88[ASN][1000 genomes]
rs1784434	0.88[ASN][1000 genomes]
rs1784435	0.88[ASN][1000 genomes]
rs1784436	0.88[ASN][1000 genomes]
rs1784437	0.88[ASN][1000 genomes]
rs1784438	0.88[ASN][1000 genomes]
rs1784439	0.81[AFR][1000 genomes]
rs1784440	0.81[AFR][1000 genomes]
rs1784441	0.81[AFR][1000 genomes]
rs1784444	0.92[AFR][1000 genomes]
rs1784445	0.92[AFR][1000 genomes]
rs1784446	0.92[AFR][1000 genomes]
rs1784447	0.92[AFR][1000 genomes]
rs1784449	0.90[AFR][1000 genomes]
rs1784451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2459479	0.81[AFR][1000 genomes]
rs2459480	0.81[AFR][1000 genomes]
rs2509015	0.81[AFR][1000 genomes]
rs2509018	0.89[ASN][1000 genomes]
rs2701961	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2846366	0.81[EUR][1000 genomes]
rs2846369	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs751547	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1815657	chr11:102413582-102490794	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102451400-102462600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:102451600-102463600	Weak transcription	NHDF-Ad	bronchial
3	chr11:102454600-102461000	Weak transcription	Primary monocytes fromperipheralblood	blood

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