Variant report

Variant	rs6911133
Chromosome Location	chr6:128970995-128970996
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11154445	0.82[EUR][1000 genomes]
rs12191852	0.84[ASN][1000 genomes]
rs12194587	0.85[ASN][1000 genomes]
rs12212602	0.80[ASN][1000 genomes]
rs1341590	0.82[EUR][1000 genomes]
rs1341591	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1341592	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1341593	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs1508436	0.83[ASN][1000 genomes]
rs2096099	0.84[ASN][1000 genomes]
rs2153706	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs2202776	0.84[ASN][1000 genomes]
rs2326737	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs471145	0.99[ASN][1000 genomes]
rs472588	0.85[ASN][1000 genomes]
rs478551	0.96[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs478649	0.84[ASN][1000 genomes]
rs479187	0.85[ASN][1000 genomes]
rs479357	0.99[ASN][1000 genomes]
rs479641	0.99[ASN][1000 genomes]
rs480169	0.83[ASN][1000 genomes]
rs482607	0.99[ASN][1000 genomes]
rs4895836	0.84[ASN][1000 genomes]
rs4897267	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs508972	0.99[ASN][1000 genomes]
rs521638	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs525293	0.96[CEU][hapmap];0.80[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs532291	0.99[ASN][1000 genomes]
rs542404	0.98[ASN][1000 genomes]
rs542925	1.00[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs545102	0.97[ASN][1000 genomes]
rs545332	0.83[ASN][1000 genomes]
rs546085	0.84[ASN][1000 genomes]
rs551729	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs562490	0.99[ASN][1000 genomes]
rs565485	0.99[ASN][1000 genomes]
rs565685	1.00[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs572745	0.86[ASN][1000 genomes]
rs575131	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62427801	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6569539	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6909897	0.84[CEU][hapmap]
rs6926043	0.83[ASN][1000 genomes]
rs6927678	0.83[ASN][1000 genomes]
rs699424	0.99[ASN][1000 genomes]
rs699425	0.85[ASN][1000 genomes]
rs699426	0.85[ASN][1000 genomes]
rs7753787	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7771173	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9321126	0.85[ASN][1000 genomes]
rs9388658	0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs9402063	0.84[ASN][1000 genomes]
rs9492031	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs969970	0.82[ASN][1000 genomes]
rs972997	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830801	chr6:128878436-129064667	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128953400-128976800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:128969600-128971200	Active TSS	Right Atrium	heart
3	chr6:128970400-128972400	Enhancers	Fetal Heart	heart
4	chr6:128970600-128971000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:128970600-128971000	Active TSS	Left Ventricle	heart
6	chr6:128970600-128971600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:128970800-128971200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:128970800-128971400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links