Variant report

Variant	rs11020863
Chromosome Location	chr11:94359989-94359990
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10831254	0.90[EUR][1000 genomes]
rs10831255	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12290280	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1940640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4127392	0.85[AFR][1000 genomes]
rs7102628	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7110865	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7124359	0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94356000-94360200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr11:94357000-94363800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:94358400-94360200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr11:94359200-94361800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr11:94359800-94368200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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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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