Variant report

Variant	rs7802922
Chromosome Location	chr7:14763050-14763051
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10215386	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10227079	1.00[AMR][1000 genomes]
rs10227542	1.00[AMR][1000 genomes]
rs10230236	1.00[AMR][1000 genomes]
rs10233046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10238594	1.00[AMR][1000 genomes]
rs10251445	1.00[AMR][1000 genomes]
rs10265238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10277933	0.95[AFR][1000 genomes]
rs10499461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12112997	1.00[AMR][1000 genomes]
rs12334082	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12334160	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16878257	1.00[AMR][1000 genomes]
rs16878259	1.00[AMR][1000 genomes]
rs16878263	1.00[AMR][1000 genomes]
rs17168342	1.00[AMR][1000 genomes]
rs17168348	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17168362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17168385	1.00[AMR][1000 genomes]
rs17168392	1.00[AMR][1000 genomes]
rs17168394	1.00[AMR][1000 genomes]
rs17168400	1.00[AMR][1000 genomes]
rs17168404	1.00[AMR][1000 genomes]
rs17168412	1.00[AMR][1000 genomes]
rs28687851	1.00[AMR][1000 genomes]
rs6948854	1.00[AMR][1000 genomes]
rs6969161	1.00[AMR][1000 genomes]
rs73682547	1.00[AMR][1000 genomes]
rs7802613	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9986816	1.00[AMR][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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887712	chr7:14717872-14829858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14712800-14775200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:14762000-14763800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:14763000-14763200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:14763000-14763400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr7:14763000-14764800	Enhancers	Colon Smooth Muscle	Colon

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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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