Variant report

Variant	rs11186651
Chromosome Location	chr10:93424883-93424884
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10881936	0.83[ASN][1000 genomes]
rs10881937	0.83[ASN][1000 genomes]
rs10881944	0.93[ASN][1000 genomes]
rs10881946	1.00[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes]
rs11186654	1.00[CHB][hapmap];0.83[JPT][hapmap];0.94[ASN][1000 genomes]
rs2421622	0.84[ASN][1000 genomes]
rs2421634	0.92[ASN][1000 genomes]
rs3980673	0.84[ASN][1000 genomes]
rs4933217	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4933686	0.84[ASN][1000 genomes]
rs7068110	0.84[ASN][1000 genomes]
rs7901243	0.95[ASN][1000 genomes]
rs7923923	0.94[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	nsv948135	chr10:93423027-93430220	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93419200-93431400	Weak transcription	Psoas Muscle	Psoas
2	chr10:93424200-93426000	Enhancers	NHDF-Ad	bronchial
3	chr10:93424600-93426800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr10:93424800-93425600	Weak transcription	Osteobl	bone
5	chr10:93424800-93449800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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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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