Variant report

Variant	rs10943057
Chromosome Location	chr6:73434273-73434274
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10455268	1.00[CHB][hapmap]
rs10484913	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10485213	0.86[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943048	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943050	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10943051	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943055	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943058	1.00[ASN][1000 genomes]
rs11759937	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12189933	1.00[CHB][hapmap]
rs12189974	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12191039	1.00[ASN][1000 genomes]
rs12191216	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12191848	1.00[ASN][1000 genomes]
rs12192751	1.00[ASN][1000 genomes]
rs12194741	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12195259	1.00[ASN][1000 genomes]
rs12197962	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12199549	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12200468	0.85[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs12200908	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12201380	1.00[ASN][1000 genomes]
rs12204139	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12204989	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12205374	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12208053	1.00[CHB][hapmap]
rs12208907	0.86[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12210850	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12211580	1.00[CHB][hapmap];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12212268	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12212419	1.00[ASN][1000 genomes]
rs12212562	1.00[CHB][hapmap]
rs12212818	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12214894	1.00[CHB][hapmap]
rs12214895	0.86[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12215865	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12374630	1.00[CHB][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12374631	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17692715	1.00[CHB][hapmap]
rs17692874	0.85[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs17692898	0.86[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs17729195	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17749408	0.86[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs17749420	0.85[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs17796704	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1928153	1.00[ASN][1000 genomes]
rs55826353	0.80[EUR][1000 genomes]
rs56316829	0.80[EUR][1000 genomes]
rs62411984	0.80[EUR][1000 genomes]
rs62411986	1.00[ASN][1000 genomes]
rs62411990	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6453591	1.00[CHB][hapmap]
rs6931918	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6935174	0.86[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs719830	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72935423	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7748594	1.00[ASN][1000 genomes]
rs7768673	1.00[CHB][hapmap]
rs7772197	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7776215	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3347486	chr6:73283590-73445976	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv830689	chr6:73385557-73544404	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv830690	chr6:73391428-73574304	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73399400-73438200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:73425200-73437600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:73429600-73434400	Weak transcription	Psoas Muscle	Psoas
4	chr6:73430600-73437600	Weak transcription	HSMM	muscle
5	chr6:73432200-73437400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr6:73434000-73434600	Enhancers	Primary B cells from cord blood	blood
7	chr6:73434000-73434600	Enhancers	Primary B cells from peripheral blood	blood
8	chr6:73434000-73434600	Enhancers	Osteobl	bone
9	chr6:73434000-73434800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:73434000-73434800	Flanking Active TSS	GM12878-XiMat	blood
11	chr6:73434200-73434600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:73434200-73434600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr6:73434200-73435200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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