Variant report

Variant	rs72787872
Chromosome Location	chr2:33907371-33907372
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11682747	0.88[ASN][1000 genomes]
rs11692842	0.90[ASN][1000 genomes]
rs2100183	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7588291	0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350238	chr2:33849408-33979026	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33905800-33907800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:33906600-33907400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:33906600-33907400	Enhancers	Fetal Brain Male	brain
4	chr2:33907200-33907400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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