Variant report

Variant	rs6936365
Chromosome Location	chr6:45586778-45586779
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:45586124..45588757-chr6:45593642..45595317,2	K562	blood:
2	chr6:45585562..45587512-chr6:45588104..45589715,2	MCF-7	breast:
3	chr6:45575640..45578537-chr6:45586483..45588913,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10080253	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12528502	0.80[ASN][1000 genomes]
rs12661055	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1491141	0.86[AFR][1000 genomes]
rs16873543	0.82[ASN][1000 genomes]
rs16873553	0.91[AFR][1000 genomes]
rs16873554	0.83[ASN][1000 genomes]
rs56083876	0.82[ASN][1000 genomes]
rs57939401	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58129892	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58939587	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59074904	0.82[ASN][1000 genomes]
rs60540355	0.83[ASN][1000 genomes]
rs60884282	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6458449	0.80[ASN][1000 genomes]
rs6458450	0.83[ASN][1000 genomes]
rs6458453	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6458454	0.85[ASN][1000 genomes]
rs6899443	0.83[ASN][1000 genomes]
rs6902401	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6914126	0.89[AFR][1000 genomes]
rs6915953	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6916895	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6917651	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6927048	0.91[AFR][1000 genomes]
rs6930188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6934210	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6938489	0.80[ASN][1000 genomes]
rs6940187	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6941971	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73738525	0.88[AFR][1000 genomes]
rs73738526	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73738527	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73738528	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7752183	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7758915	0.83[ASN][1000 genomes]
rs7759415	0.83[ASN][1000 genomes]
rs7763886	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7766534	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7768962	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9296462	0.83[ASN][1000 genomes]
rs9463108	0.83[ASN][1000 genomes]
rs9472521	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9472524	0.83[ASN][1000 genomes]
rs9472525	0.83[ASN][1000 genomes]
rs9472527	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9472531	0.80[ASN][1000 genomes]
rs9472532	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][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	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv427755	chr6:45474631-45627025	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45579000-45587800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:45582000-45587200	Weak transcription	NHLF	lung
3	chr6:45582600-45587000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:45582600-45587400	Weak transcription	NHDF-Ad	bronchial
5	chr6:45582800-45588200	Weak transcription	Fetal Lung	lung
6	chr6:45583200-45587600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:45583200-45587800	Weak transcription	NHEK	skin
8	chr6:45583400-45587400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:45583600-45587000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:45583600-45587600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:45584600-45588600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:45584600-45589000	Enhancers	HSMM	muscle
13	chr6:45585600-45587400	Weak transcription	HSMMtube	muscle
14	chr6:45585800-45587000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr6:45585800-45587400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:45585800-45587400	Weak transcription	NH-A	brain
17	chr6:45586000-45587200	Weak transcription	Osteobl	bone
18	chr6:45586000-45587600	Weak transcription	HMEC	breast
19	chr6:45586000-45588000	Weak transcription	Hela-S3	cervix
20	chr6:45586400-45587600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:45586400-45587800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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