Variant report

Variant	rs2221724
Chromosome Location	chr11:109018174-109018175
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11212954	0.81[ASN][1000 genomes]
rs11212956	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1509731	0.81[ASN][1000 genomes]
rs1553769	0.81[ASN][1000 genomes]
rs4754384	0.81[ASN][1000 genomes]
rs61913335	0.81[ASN][1000 genomes]
rs61913336	0.81[ASN][1000 genomes]
rs61913337	0.81[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	nsv1040650	chr11:108859584-109174553	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:109012000-109021200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr11:109012000-109021400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:109012800-109018800	Weak transcription	Fetal Heart	heart

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

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