Variant report

Variant	rs7822201
Chromosome Location	chr8:36077059-36077060
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10103388	0.83[ASN][1000 genomes]
rs10111851	0.83[ASN][1000 genomes]
rs2702470	0.81[ASN][1000 genomes]
rs2702491	0.83[ASN][1000 genomes]
rs2702496	0.83[ASN][1000 genomes]
rs2843885	0.82[ASN][1000 genomes]
rs2843886	0.83[ASN][1000 genomes]
rs2843887	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533420	chr8:35358115-36227536	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1024552	chr8:35655964-36210907	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539548	chr8:35655964-36210907	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv890718	chr8:35948467-36224134	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv819958	chr8:36073740-36080027	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv2422113	chr8:36075155-36078341	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
7	nsv442104	chr8:36075155-36078341	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
8	nsv824596	chr8:36075478-36078619	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
9	nsv824597	chr8:36075478-36079997	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
10	nsv515078	chr8:36075678-36078358	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36076600-36078600	Weak transcription	Adipose Nuclei	Adipose

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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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