Variant report

Variant	rs6506536
Chromosome Location	chr18:7845327-7845328
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10502362	0.89[CEU][hapmap]
rs1117814	0.82[EUR][1000 genomes]
rs12457653	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs12608415	0.93[EUR][1000 genomes]
rs12965898	0.89[CEU][hapmap]
rs1348104	0.93[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs1348407	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1348408	0.90[EUR][1000 genomes]
rs1440995	0.89[CEU][hapmap]
rs1440999	0.89[CEU][hapmap]
rs1441000	0.89[CEU][hapmap]
rs1441001	0.88[CEU][hapmap]
rs1443607	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443608	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443609	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443610	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443611	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443612	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443613	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443614	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1443616	0.92[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1530389	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1561654	0.94[EUR][1000 genomes]
rs1822456	0.82[EUR][1000 genomes]
rs1838187	0.89[EUR][1000 genomes]
rs2009770	0.89[CEU][hapmap]
rs2099790	0.96[CEU][hapmap];0.94[EUR][1000 genomes]
rs2197010	0.82[EUR][1000 genomes]
rs2377575	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2377576	0.82[EUR][1000 genomes]
rs331415	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs331418	0.81[CEU][hapmap]
rs36188935	0.82[EUR][1000 genomes]
rs4797302	0.82[EUR][1000 genomes]
rs4798598	0.81[CEU][hapmap]
rs4798599	0.82[EUR][1000 genomes]
rs4798600	0.82[EUR][1000 genomes]
rs4798601	0.82[EUR][1000 genomes]
rs4798602	0.82[EUR][1000 genomes]
rs4798603	0.82[EUR][1000 genomes]
rs6506535	0.92[CEU][hapmap];0.80[AMR][1000 genomes]
rs6506538	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs671369	0.89[CEU][hapmap]
rs7227367	0.82[EUR][1000 genomes]
rs7235300	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs7239136	0.83[CEU][hapmap]
rs7240568	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7243673	0.85[CEU][hapmap]
rs727949	0.93[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs727951	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs8083298	0.82[EUR][1000 genomes]
rs8089088	0.82[EUR][1000 genomes]
rs8095400	0.82[EUR][1000 genomes]
rs8095467	0.82[EUR][1000 genomes]
rs9944547	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv458016	chr18:7488133-7934001	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv576399	chr18:7488133-7934001	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking 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	6 gene(s)	inside rSNPs	diseases
4	esv2762810	chr18:7492090-7924728	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1062911	chr18:7561991-8088274	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv543637	chr18:7561991-8088274	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1064345	chr18:7562051-8088274	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv543638	chr18:7562051-8088274	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv576425	chr18:7747873-7859757	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7844000-7847200	Weak transcription	Gastric	stomach
2	chr18:7844000-7855200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr18:7844200-7845800	Weak transcription	Left Ventricle	heart
4	chr18:7844200-7845800	Weak transcription	Lung	lung
5	chr18:7844200-7848400	Weak transcription	Ovary	ovary
6	chr18:7844600-7845800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr18:7844600-7855200	Weak transcription	Aorta	Aorta
8	chr18:7844800-7847600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr18:7844800-7847800	Weak transcription	Fetal Lung	lung
10	chr18:7844800-7854200	Weak transcription	A549	lung
11	chr18:7844800-7856600	Weak transcription	Thymus	Thymus
12	chr18:7845000-7848000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr18:7845000-7856800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr18:7845200-7846400	Weak transcription	Fetal Heart	heart
15	chr18:7845200-7851400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links