Variant report

Variant	rs7756695
Chromosome Location	chr6:48715166-48715167
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2474493	1.00[AMR][1000 genomes]
rs2490129	1.00[AFR][1000 genomes]
rs2490130	1.00[AMR][1000 genomes]
rs2495858	1.00[AMR][1000 genomes]
rs2495919	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2495921	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2495932	1.00[AMR][1000 genomes]
rs2997373	1.00[AMR][1000 genomes]
rs4236099	0.86[AFR][1000 genomes]
rs4236100	0.86[AFR][1000 genomes]
rs4499933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4715096	1.00[AMR][1000 genomes]
rs9381692	1.00[AMR][1000 genomes]
rs9473470	0.86[AFR][1000 genomes];1.00[AMR][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	nsv1033151	chr6:48067287-48797029	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538217	chr6:48067287-48797029	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2752125	chr6:48575963-48718589	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv949690	chr6:48595821-49289855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv885879	chr6:48634956-48730669	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:48714200-48715400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:48714600-48715200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:48714600-48715200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:48714600-48715400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr6:48714600-48715400	Enhancers	HMEC	breast
6	chr6:48714600-48715600	Enhancers	Fetal Lung	lung
7	chr6:48714600-48715600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr6:48714600-48715800	Enhancers	Hela-S3	cervix
9	chr6:48714800-48715200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:48715000-48715400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:48715000-48715400	Enhancers	NHLF	lung
12	chr6:48715000-48715400	Enhancers	Osteobl	bone

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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