Variant report

Variant	rs1570075
Chromosome Location	chr6:79315357-79315358
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1012026	0.94[ASN][1000 genomes]
rs1012027	0.96[ASN][1000 genomes]
rs10455349	0.95[ASN][1000 genomes]
rs10806133	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10943547	0.98[ASN][1000 genomes]
rs10943548	0.96[ASN][1000 genomes]
rs10943549	0.94[ASN][1000 genomes]
rs12197137	0.95[ASN][1000 genomes]
rs12201840	0.93[ASN][1000 genomes]
rs12209692	0.96[ASN][1000 genomes]
rs12210711	0.95[ASN][1000 genomes]
rs12213548	0.94[ASN][1000 genomes]
rs12530353	0.95[ASN][1000 genomes]
rs12530368	0.89[ASN][1000 genomes]
rs1395446	0.96[ASN][1000 genomes]
rs1395447	0.98[ASN][1000 genomes]
rs1407102	0.94[ASN][1000 genomes]
rs1567095	0.95[ASN][1000 genomes]
rs1567096	1.00[CHB][hapmap];0.91[JPT][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1567097	0.96[ASN][1000 genomes]
rs16890224	0.96[ASN][1000 genomes]
rs16890230	0.96[ASN][1000 genomes]
rs1995650	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs2063045	0.95[ASN][1000 genomes]
rs2202588	0.82[ASN][1000 genomes]
rs2321764	0.94[ASN][1000 genomes]
rs236852	0.84[ASN][1000 genomes]
rs236853	0.95[ASN][1000 genomes]
rs236855	0.94[ASN][1000 genomes]
rs236859	0.95[ASN][1000 genomes]
rs236882	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs236884	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs236886	0.96[ASN][1000 genomes]
rs5018093	0.93[ASN][1000 genomes]
rs699182	0.96[ASN][1000 genomes]
rs717364	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs7755578	0.93[ASN][1000 genomes]
rs7763429	0.86[ASN][1000 genomes]
rs9361413	0.86[ASN][1000 genomes]
rs9361414	0.86[ASN][1000 genomes]
rs984157	0.98[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	nsv886235	chr6:78861808-79369972	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv604011	chr6:79042990-79455282	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv886300	chr6:79129963-79341891	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv522646	chr6:79185106-79333988	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1028767	chr6:79200713-79341224	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79309800-79324800	Weak transcription	Aorta	Aorta
2	chr6:79313600-79316800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:79314400-79315800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:79314800-79315600	Weak transcription	HSMMtube	muscle
5	chr6:79315000-79315600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:79315000-79315600	Enhancers	A549	lung
7	chr6:79315000-79315600	Enhancers	HSMM	muscle
8	chr6:79315000-79315600	Flanking Active TSS	NHLF	lung
9	chr6:79315000-79315800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:79315000-79315800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:79315000-79315800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:79315000-79315800	Flanking Active TSS	Osteobl	bone
13	chr6:79315000-79316000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:79315000-79316200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr6:79315000-79316200	Flanking Active TSS	HUVEC	blood vessel
16	chr6:79315200-79315400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:79315200-79315400	Active TSS	NH-A	brain
18	chr6:79315200-79315800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:79315200-79315800	Flanking Active TSS	HMEC	breast
20	chr6:79315200-79315800	Flanking Active TSS	NHDF-Ad	bronchial
21	chr6:79315200-79315800	Flanking Active TSS	NHEK	skin
22	chr6:79315200-79316200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:79315200-79317400	Enhancers	Hela-S3	cervix

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