Variant report

Variant	rs10816591
Chromosome Location	chr9:110700994-110700995
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10512375	0.83[YRI][hapmap]
rs10521087	0.86[ASW][hapmap];0.92[LWK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs10759269	0.93[EUR][1000 genomes]
rs10816590	0.92[EUR][1000 genomes]
rs10816592	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10816593	1.00[CHB][hapmap];0.88[JPT][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10816596	0.85[EUR][1000 genomes]
rs12343242	0.95[YRI][hapmap]
rs12351443	0.89[AFR][1000 genomes]
rs34844672	0.89[AFR][1000 genomes]
rs6477606	1.00[LWK][hapmap];0.83[MKK][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes]
rs7026539	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.97[GIH][hapmap];0.82[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7041168	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7867441	0.89[AFR][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	nsv893701	chr9:110650482-110709587	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110694000-110701000	Weak transcription	Spleen	Spleen
2	chr9:110695800-110701200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:110695800-110705200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr9:110696000-110701000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr9:110696200-110707800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:110700400-110702200	Enhancers	Primary hematopoietic stem cells	blood

Quick Search:

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

what's new

Quick links